Unit 1 Student Notes Complete
Unit 1 Student Notes Complete
Unit 1 Student Notes Complete
AP Biology
Unit 1
Student Notes
Unit 1 Student Notes Page 2
Table of Contents Link
Table of Contents
Step 4: Experiment
A. The scientist must develop and follow a procedure that anyone can follow.
1. Use precise directions.
2. Include a detailed materials list.
3. The outcome must be quantifiable (measurable).
4. The experiment must have a control group.
a. The control group may be a “no treatment” or an “experimenter selected” group to use
as a standard of comparison for the independent variable.
b. The control group may be a “no treatment” or an “experimenter selected” group to use
as a standard of comparison for the independent variable.
A negative control group is a control group that is not exposed to the experimental
treatment or to any other treatment that is expected to have an effect.
For example, imagine that you wanted to know if some lettuce carried bacteria. You set
up an experiment in which you wipe lettuce leaves with a swab, wipe the swab on a
bacterial growth plate, incubate the plate, and see what grows on the plate. As a
negative control, you might just wipe a sterile swab on the growth plate. You would not
expect to see any bacterial growth on this plate, and if you do, it is an indication that
your swabs, plates, or incubator are contaminated with bacteria that could interfere
with the results of the experiment.
Unit 1 Student Notes Page 5
Table of Contents Link
A positive control group is a control group that is not exposed to the experimental
treatment but that is exposed to some other treatment that is known to produce the
expected effect.
As a positive control, you might swab an existing colony of bacteria and wipe it on the
growth plate. In this case, you would expect to see bacterial growth on the plate, and if
you do not, it is an indication that something in your experimental set-up is preventing
the growth of bacteria. Perhaps the growth plates contain an antibiotic or the incubator
is set to too high a temperature.
Example: In the miracle-gro experiment described above, the negative control group would
consist of plants that are not exposed to any miracle-gro.
c. The control group is exposed to all of the same factors as the experimental group(s) except for
the independent variable being tested.
Experimental group – group or groups that have the independent variable
applied/manipulated.
Example: In the miracle-gro experiment, the experimental group would consist of a
group of plants that are treated with miracle-gro. We might treat different subgroups
with different amounts of miracle-gro to test the effect of concentration.
Constants – all the factors that the experimenter attempts to keep the same/control in all of the
groups in the experiment.
Example: In the miracle-gro experiment, we would want to ensure that all of the plants are of
the same species, growing in the same type of soil, exposed to the same amount of light, given
the same amount of water, and grown at the same temperature.
Step 7: Conclusion
A. The written results of the experiment.
B. Include a statement if the hypothesis was supported or refuted.
C. Make recommendations for further study and possible improvements to the procedure.
Graphs and charts communicate information visually. They can show patterns, help scientists identify correlations,
and get the point of the experiment across quickly.
The independent variable is plotted on the x-axis
The dependent variable is plotted on the y-axis.
The mnemonic DRY MIX, for “dependent, responding, y-axis” and “manipulated, independent, x-axis,” can help
you remember this pattern.
Label both axes (independent variable on the X-axis and dependent variable on the Y-axis)
Provide a descriptive title. Use the pattern, “The Effect of the independent variable on the dependent variable”.
For example if you were graphing the miracle-gro concentration against plant height. The title of the graph might
be “The Effect of Miracle-Gro Concentration on Plant Height”.
If the instruction is to plot rather than graph the data points, no line needs to be drawn.
If a line is drawn, do not extend the line beyond the last point plotted (unless asked to make a prediction) or connect
the line from the origin (unless there is a time zero reading.)
If multiple lines are drawn on the same graph, label each line clearly.
A) Line Graph: are used for looking at the relationship between two continuous types of data. Typically, both the
independent and dependent variables are numerical.
B) Bar Graphs: are used for making comparisons between discrete cases or to look for trends, such as over space
or time. The independent variable is usually a category and the dependent variable is usually an average,
percentage, or frequency.
C) Scatter Plot: Scatter plots are used for examining relationships between two types of data. These are very
similar to line graphs, just without the line.
Line graphs provide an excellent way to map independent and dependent variables that are both quantitative. When
both variables are quantitative, the line segment that connects two points on the graph expresses a slope, which can
be interpreted visually relative to the slope of other lines or expressed as a precise mathematical formula. Scatter
plots are similar to line graphs in that they start with mapping quantitative data points. The difference is that with a
scatter plot, the decision is made that the individual points should not be connected directly together with a line but,
instead express a trend. This trend can be seen directly through the distribution of points or with the addition of a
regression line or line of best fit.
The AP Biology exam often asks students to find the rate of a process or reaction between two points on a graph.
In order to find the rate, calculate the slope of the best fit line that connects the two points. Use m=y 2-y1/x2- x1
Unit 1 Student Notes Page 7
Table of Contents Link
Be sure to include a unit with your answer. The unit for the slope/rate should be the y axis unit divided by the x
axis unit.
Example:
You are asked to calculate the yeast population growth rate between t=5 hours and t=10 hours.
First, determine your coordinates at those times. The coordinates should be (5, 3.5) and (10, 25).
You must write all answers in complete sentences! There is room on the test for you to create an outline to
guide your answer, but outlines are not graded. That being said, perfect essay writing is not expected. There are
no deductions for grammar or spelling mishaps (provided the spelling is close enough to determine the word
you are trying to write).
Diagrams are helpful. However, if you draw a diagram, be sure to refer to it in your essay. You will not earn
points for diagrams that stand by themselves. You must explain all diagrams and drawings.
Points are not deducted from your essay score if you give an incorrect statement. You just do not
receive points for incorrect statements. However, you must be careful not to contradict yourself. If you
state something correctly but then later state the opposite, you will not earn the point.
Use graphs or diagrams when it will enhance your essay response. However, unless the prompt
specifically asks for drawings/graphs, every thought you hope to convey must also be put in writing.
Label all graphs correctly.
Include a graph title.
Include a key/legend which clearly identifies lines and data points.
Label axes (including units).
Unit 1 Student Notes Page 9
Table of Contents Link
Tips for AP Lab Free Response Questions:
Design an Experiment Free Response Questions
The AP Biology exam will often ask you to design an experiment to address a certain topic/question. When asked
to design an experiment, always include the following elements in your answer:
Form a concise hypothesis which is testable. State It Clearly! Use the if…then format. For example: If tomato
plants are exposed to increased amounts of Miracle-Gro, then they will grow taller.
Describe the control group that you will use for comparison with the experiment.
Describe the basic procedure that you will use. Describe the measurements that you will take, the # or subjects
that you will use, and how the subjects were assigned to either the control or experimental groups. This should
usually be random.
Describe the statistical tests that you will use to interpret the data (Chi Square, rate determination…).
Make a prediction about the expected outcome and a rationale for your prediction.
Don’t over-complicate the mean calculation. The mean is simply the average of your sample.
The mean summarizes the entire sample and might provide an estimate of the entire population’s true mean.
The sample size (n) refers to how many members of the population are included in the study. Sample size is important
when students try to estimate how confident they can be that the sample set they are trying to analyze represents the
entire population.
Both the standard deviation measure and the standard error measure define boundaries of probabilities.
The sample standard deviation (S) is a tool for measuring the spread (variance) in the sample population, which in turn
provides an estimate of the variation in the entire sample set. A large sample standard deviation indicates that the data
have a lot of variability. A small sample standard deviation indicates that the data are clustered close to the sample
mean.
The AP Biology formula sheet lists the following formula for calculating standard deviation:
Unit 1 Student Notes Page 12
Table of Contents Link
Most likely, you will not be asked to calculate the standard deviation on an AP exam, but you will be expected to be able
to interpret its meaning and be able to use it to analyze your data and construct appropriate graphs.
In a normal distribution, a little more than two-thirds of the data points will fall between +1 standard deviation and −1
standard deviation from the sample mean. More than 95% of the data falls between ±2 standard deviations from the
sample mean.
Sample standard error (SEx) is a statistic that allows students to make an inference about how well the sample mean
matches up to the true population mean. The standard error of the mean utilizes the standard deviation of the sample
and the sample size to estimate how closely the sample data approximates the data that would be collected if the entire
population were measured. If one were to take a large number of samples (at least 30) from a population, the means
for each sample would form an approximately normal distribution—a distribution of sample means. Normally, you
would not do hundreds of individual investigations on a population. This distribution of sample means, then, is a
theoretical construct that helps us define our boundaries of confidence in our sample. This distribution also has
parameters, such as a standard deviation. Standard error is the equivalent of the standard deviation of the sampling
distribution of the means and is calculated from the following formula:
You will probably not be asked to calculate the standard error of the mean on an AP Biology exam, but you will be
expected to use the standard error to analyze your data and construct appropriate graphs.
An interval within ±1 SEx of the sample mean describes the range of values about which an investigator can have
approximately 67% confidence that the range includes the true population mean. Even better, a sample interval within
Unit 1 Student Notes Page 13
Table of Contents Link
±2 SEx of the sample mean defines a range of values with approximately a 95% certainty that the true population mean
falls within the interval. This interval is often referred at as a 95% confidence interval. You will be asked to graph 95%
confidence intervals on a regular basis in this course.
The 95% confidence interval technique is an inference; it is a statistic that allows investigators to gauge just how good
their estimate of the true population mean actually is. With this understanding, the investigator can establish ahead of
time a reasonable sample size for this population and the degree of confidence needed. Note: The larger the sample
size, the smaller the standard error and the more confident the researcher can be about the reliability of the data.
Creating and Interpreting Graphs with Error Bars
The Standard Error of the Mean and the 95% Confidence Interval are used to construct error bars for graphs showing
the mean values of data sets. In AP Biology, the error bars usually show the range 2 standard errors above and 2 below
the mean value.
To create a graph with error bars, graph the means of each data set using a bar chart. Starting at the mean of the first
bar, move directly up 2 times the SEx. At that point, draw a horizontal line centered over the bar. Go back to the mean,
and move directly down 2 times the SEx. Again, draw a horizontal line that is in line with the line you drew above the
bar. Connect the two horizonal lines with a vertical line through their centers.
Repeat the process for the other bars included in the chart.
The vertical space between the two horizontal lines represents a 95% confidence interval. This means that you can be
95% sure that the mean for the entire population falls within this interval.
As a researcher, you may want to use your collected data to compare samples/groups and to determine if the groups
are “significantly different”.
A "significant difference" means that the results that are seen in the data are most likely not due to chance or sampling
error. In any experiment or observation that involves sampling from a population, there is always the possibility that an
observed effect could have occurred due to sampling error alone. But if a result is "significant," the investigator may
conclude that the observed effect actually reflects the characteristics of the population rather than just sampling error
or chance.
The standard error bars on a graph can be used to get a sense for whether or not a difference in two groups/samples is
significant. Look for overlap between the error bars:
When errors bars overlap quite a bit, it's likely that the difference between the two groups is not statistically significant
and the differences are probably due to chance or sampling error. You must actually perform a statistical test to draw a
valid conclusion, but in AP Biology you can simply say that if the error bars overlap that the two groups/samples are
not statistically different.
On the other hand, if there is no overlap between the error bars, the differences between the two groups is likely to
be statistically significant.
Answer to Example:
Unit 1 Student Notes Page 15
Table of Contents Link
Died in Drought Survived Drought
mean 10.4 10.825
S 0.365148 0.242773
The mean beak depth after the drought was different in a statistically significant amount from the beak depth before the
drought. This can be determined by looking at the error bars for the two conditions. Since the error bars don’t overlap,
the differences are likely to be statistically significant.
10.9
Mean beak
depth
10.8 (mm)
10.7
10.6
10.5
10.4
10.3
10.2
10.1
1 2
Died in Drought Survived
Drought
Note: To add error bars to an excel graph, click on the “chart elements” button. From the drop down menu, choose
standard error.
Unit 1 Student Notes Page 16
Table of Contents Link
Hypothesis Testing
A hypothesis is a statement explaining that a causal relationship exists between an underlying factor (variable) and an
observable phenomenon. Often, after making an observation, you might propose some sort of tentative explanation for
the phenomenon; this could be called your working hypothesis. Because absolute proof is not possible, statistical
hypothesis testing focuses on trying to reject a null hypothesis.
A null hypothesis (H0) is a statement explaining that the underlying factor or variable is independent of the observed
phenomenon—there is no causal relationship.
Stated another way, a null hypothesis (H0) is usually a statement asserting that there is no difference or no association
between variables. The null hypothesis is a tool that makes it possible to use certain statistical tests to figure out if
another hypothesis of interest is likely to be accurate or not. For example, if you were testing the idea that sugar makes
kids hyperactive, your null hypothesis might be that there is no difference in the amount of time that kids previously
given a sugary drink and kids previously given a sugar-substitute drink are able to sit still. After making your
observations, you would then perform a statistical test to determine whether or not there is a significant difference
between the two groups of kids in terms of time spent sitting still.
The alternative hypothesis (HA) to the null hypothesis might be that there is a difference between the two groups of kids
in terms of time spent sitting still. Usually (but not always), an investigator is trying to find an alternative to the null
hypothesis—evidence that supports the alternative hypothesis by rejecting the null (based on statistical tests). If the
null hypothesis (that there is no difference between the two groups of kids in terms of time spend sitting still) can be
rejected, then that is support for this alternative hypothesis.
It is important to realize that hypothesis testing does not allow proof, or even acceptance, of the alternative to the null
hypothesis. Typically, the decision comes down to whether there is enough evidence to reject the null hypothesis. If
Unit 1 Student Notes Page 17
Table of Contents Link
evidence to reject the null hypothesis is sufficient, what can be said is that the investigator rejects the null hypothesis
—not that the investigation has proven the alternative hypothesis. This is a crucial concept for students to understand.
In data analysis, investigators determine the size and confidence they have in various population parameters that were
measured, counted, or calculated during the course of the investigation. Hypothesis testing asks the question, Is there
something to these measurements? or Is the effect real?
Types of Statistical Tests
There are a wide range of statistical tests which can be used for hypothesis testing. For AP Biology, we will focus on only
two of these methods: chi square analysis and the t-test.
Chi Square Analysis
The Chi-square test is a statistical method that makes a comparison between the data collected in an experiment and
the data an investigator expected to find. The Chi square test is a way to evaluate the variability that is always present
in the real world to get an idea if the difference between the real and expected results is due to random chance or if
some other factor is involved.
Chi square analysis can be used when you are comparing two or more categories of data. In AP Biology, the categories
will usually be the observed and expected data. The actual data under these categories will typically be in the form of
either counts or percentages. Chi square analysis should not be used to compare averages. For example, chi square
analysis can be used to test how well the results of genetic crosses fit predicted outcomes based on Mendel’s laws of
inheritance or to see how well measured gene frequencies in a population match up to Hardy-Weinberg predictions.
When the Chi-square test is applied in these kinds of analyses, the goal is to determine whether or not the variation in
the results from the expected values is due to chance. In these analyses, students are trying to confirm a theoretical
expectation about their data, and they hope to quantify the contribution due to chance events. Here researchers hope
to fail to reject the null hypothesis, i.e., that there is no evidence of a significant difference between the expected and
observed results. This approach might also be used in the M& M lab in which students compare the percentages of
M&Ms of each color in a bag to the theoretical percentages produced at the factory.
In other investigations, however, students may ask a question that requires a different application of the Chi-square test.
For example, in a pill bug environmental choice experiment, students may wish to know if pill bugs actually choose one
environment over another, or whether they just randomly move about. With this type of investigation, students are
trying to discover and verify that an actual pattern exists as opposed to the random variation that often characterizes
natural systems. Here students hope to reject the null hypothesis, indicating that their observed results are significantly
different from the ones they expected.
The Chi Square statistic can be calculated using the table formula included on the next page. My advice for calculating
chi square is to setup a table like the one included at the bottom of the next page.
Unit 1 Student Notes Page 18
Table of Contents Link
Let’s walk you through the process of calculating chi square by working through an example problem.
• A student wanted to know if pillbugs have a preference for wet or dry environments. The student setup a choice
chamber with a wet and a dry side. He placed 10 pillbugs on each side of the chamber and after 2 hours found
14 pillbugs on the wet side and 6 on the dry side.
• The student’s null hypothesis was that pillbugs had no preference for either wet or dry
Unit 1 Student Notes Page 19
Table of Contents Link
• His phenotypes or groups for this test are “wet” and “dry”
• His observed values are “14” on the wet side and “6” on the dry side.
• Fill in the columns in the chart by performing the mathematical calculations shown at the top of each row. See
the chart below as an example.
• The chi square statistic is calculated by find the sum of the last column in the table. Remember that chi square is
equal to:
• There are two different ways to interpret the meaning of the chi square statistic. One way is to compare it to a
critical value. Use the chi square table, included above to find this critical value. First, determine your degrees
of freedom. The degrees of freedom are equal to your number of phenotypes/categories minus one. In this
case, our degrees of freedom are equal to 1.
• We are always going to use the 0.05 significance level in Biology. The significance level, also denoted as alpha or
α, is the probability of rejecting the null hypothesis when it is true. For example, a significance level of 0.05
indicates a 5% risk of concluding that a difference exists when there is no actual difference. This is essentially an
error range.
• Use the 0.05 significance level and the 1 degree of freedom to find a critical value of “3.84” in the chi square
table.
• Compare the critical value “3.84” to the chi square statistic (3.2) that we calculated. If the chi square statistic is
greater than the critical value, we will reject the null hypothesis. In this experiment, the chi square statistic is
less than the critical value. This means that we must fail to reject the null hypothesis. This essentially means
that the differences between our observed and expected values are small and likely due to chance.
• The other way to interpret the chi square statistic is to use the p-value approach. Move along row 1 (1 degree
of freedom) in the chi square distribution table included below until you can find the Chi-square value of 3.2. It is
somewhere between the 0.10 column and the 0.05 column. This means that the p-value for this data is between
0.10 and 0.05. Remember, the probability of whether the results of an investigation differ from the null results
by chance alone is called the p-value. A p-value of 0.05 means that there is a 5% chance that the difference
between the observed and the expected data is a random difference and a 95% chance that the difference is
real and repeatable—in other words, a significant difference. Therefore, if an investigator’s p-value is greater
than 0.05, he or she would fail to reject the null hypothesis—that the difference between the observed results
and the expected results is due to random chance and is not significant. Our data fall into this category. This
means that our data doesn’t indicate that pillbugs prefer a wet environment over a dry environment. On the
other hand, if the p-value had been less than 0.05, we would have rejected the null hypothesis. This would
have indicated that the differences between our observed and expected data were significant and likely due to
Unit 1 Student Notes Page 20
Table of Contents Link
something other than chance. This same p-value approach is used with the t-test and ANOVA testing.
• See the chi square Powerpoint and chi square video for more practice with chi square analysis.
t-Test
A t-test is commonly used to determine whether the mean of a population significantly differs from the mean of
another population. This is useful if you need to compare the means of control and experimental groups. In most cases
in AP Biology, you are going to assume that the data is parametric (follows a normal distribution) and that the two
samples are independent of each other.
An excellent place to use the t-test in AP Biology would be in comparing the mean number of trichomes in the different
fast plant generations (from the Artificial Selection Lab). We will use the t-test to analyze some simulated artificial
selection lab data. Our null hypothesis for this test is that, “The mean number of trichomes in the generation 2 sample is
the same as the mean of the generation 1 sample.”
Calculation steps:
1. Calculate the mean of each sample population and subtract one from the other. Take the absolute value of this
difference.
2. Calculate the standard error, SE. To compute it, calculate the variance (standard deviation squared) (S 2) of each
sample, and divide it by the number of measured values in that sample (n, the sample size). Add these two values and
then take the square root.
3. Divide the difference between the means by the standard error to get a value for the t-statistic. This calculation yields
“2.9417” for our data.
4. Compare the calculated value to the appropriate critical t-value in the table included below. Table 8 shows the
critical values for different degrees of freedom at a significance value of 0.05. The degrees of freedom are calculated by
adding the number of data points in the two groups combined, minus 2. In our situation that would be (7 + 7 -2). We
should use 12 degrees of freedom for our trichome data. Note that you do not have to have the same number of data
points in each group. If the calculated t-value is greater than the appropriate critical t-value, this indicates that you
should reject the null hypothesis and that you have enough evidence to support the hypothesis that the means of the
two samples are significantly different at the probability value listed (in this case, 0.05). If the calculated t is smaller
than the critical value, then you cannot reject the null hypothesis that there is no significant difference.
Unit 1 Student Notes Page 22
Table of Contents Link
In our example the t-test statistic of “2.9417” is greater than the critical value of “2.18”. This means that we should
reject the null hypothesis. There is evidence that the mean number of trichomes in the generation 2 sample is different
than the mean number of trichomes in the generation 1 sample.
Just as there is with chi square analysis, there is another way to interpret the t-test data using p-values. Move along row
12 (12 degrees of freedom) in the t distribution table included below until you can find the t value of .2.9417. It is
somewhere between the 0.02 column and the 0.01 column. This means that the p-value for this data is between 0.02
and 0.01. Remember, the probability of whether the results of an investigation differ from the null results by chance
alone is called the p-value. A p-value of 0.05 means that there is a 5% chance that the difference between the observed
and the expected data is a random difference and a 95% chance that the difference is real and repeatable—in other
words, a significant difference. Therefore, if an investigator’s p-value is greater than 0.05, he or she would fail to reject
the null hypothesis—that the difference between the observed results and the expected results is due to random chance
and is not significant. In our case, the p-value is less than 0.05. This means that we should reject the null hypothesis
and that the differences between the means of the two generations is statistically different. There is less than a 5%
chance that the differences between the means is due to chance.
Unit 1 Student Notes Page 23
Table of Contents Link
Visit the following links for more information about the t-test.
AP Biology Statistics Teacher Guide
AP Quantitative Skills Guide
Bozeman Science t-test video
Performing a t-test in Google Sheets
The t-test calculations are very laborious. In most cases, you won’t do them by hand. Below are directions for
calculating a t-test with Excel, a TI calculator, and Google Sheets.
Excel calculates a T-test in a slightly different way. Rather than giving you the t value and comparing it to a table of
critical values, Excel simply tells you the probability that the means are different simply due to chance, the “P value.”
Follow these steps to calculate a P value using a t-test with Excel:
1. Create two columns, side by side, for the data of interest. Each sample’s data should be in separate columns
2. Click on another blank cell where you wish the P value to appear.
3. Then click “fx” on the Excel Formulas toolbar.
4. In the box, search for the "T test" function and choose “T.TEST" from the list. Hit OK. You will need to set the t-
test parameters:
Unit 1 Student Notes Page 24
Table of Contents Link
For “Array1” highlight the data from one sample; for “Array2”, highlight the data in the second sample.
Enter “2” in the box for “Tails.”
Lastly, you will have to select the “Type” of t-test. For our purposes, we will mostly use type “2.” Although, if
you are measuring the same sample at two points in time (for example before and after treatment) then you
would have a type "1."
5. After answering these questions click “OK” and the P value will appear. The P value will fall between zero and one.
Unit 1 Student Notes Page 25
Table of Contents Link
What does my P value mean? Excel gives the chance that the differences between the two samples are due to random
chance alone. If Excel calculates a P value of 0.22, it means that there is a 22% likelihood that the difference in the
means of your two data sets is due to random chance. If the calculated p-value is .05 or less the differences between
the two groups is significant and you should reject the null hypothesis. If the P value is greater than 0.05, we can
accept the null hypothesis and conclude that there is no significant difference between the two groups.
1. Enter the data from your two samples in two separate columns.
2. Insert the formula: =TTEST(A1:A4, B1:B4, 2, 2). Replace A1:A4 with your data from the first sample and
B1:B4 with your data from the second sample.
3. As with Excel, this calculation will give you the p-value, not the t-test statistic. If the p-value is less than
0.05, reject the null hypothesis. If the p-value is greater than 0.05, accept the null hypothesis.
AP Biology
Biochemistry – Chemistry Basics
Atom
The smallest unit of an element that maintains the chemical properties of the element.
Unit 1 Student Notes Page 26
Table of Contents Link
Subatomic Particles
Proton – Subatomic particles that carry a positive charge. They are located in the nucleus of an atom.
The number of protons never changes in an element. The number of protons determines the
identity of the element and defines the atomic number of the element.
Neutron - These particles carry NO charge (are neutral). They are also located in the nucleus of
an atom and are similar in size to the proton.The number of neutrons can change. (Atoms of the
same element with different numbers of neutrons are called Isotopes.)
Electrons - These subatomic particles carry a negative charge. They are located in the “Electron cloud”. The
electrons are attracted to the positive protons in the nucleus, but can move within the electron cloud. The
number of electrons associated with an atom can change. (Atoms with different numbers of electrons than the
normal amount for that element are called Ions.)
Molecule
Two or more atoms that are covalently bonded together.
E levels or e- shells – Where the electrons are located within an atom or molecule.
Adding energy to the electrons makes them move farther out, away from the nucleus; losing energy causes
them to move inward, toward the nucleus.
Valence Shell- Where the outer most electrons are located on an atom.
Valence e- - Refers to the outer most electrons. (These are the most important for chemical bonds and the
chemical properties of an element or molecule.) Most elements need 8 valence electrons (an octet) in order
to be chemically stable. Atoms react with other elements in order to obtain a total of 8 valence electrons and
to become chemically stable.
Covalent Bonds
A type of intramolecular bond.
Results from the sharing of valence electrons between atoms.
Atoms held together by covalent bonds are called molecules.
Polar molecules carry a slight electrical charge at opposite poles (poles refers to the “ends” of the
molecule) and non-polar molecules do not have an electrical charge.
Electronegativity
Refers to an atom’s desire to acquire electrons.
Hydrogen is the least electronegative atom.
Oxygen and Nitrogen are the most biologically important molecules with a high
electronegativity.
Molecules which contain oxygen and nitrogen are likely to be polar.
Ionic Bonds
Ionic bonds form between metal and non-metal atoms.
They form when the metal atoms loses electrons and the non-metal atom gains electrons.
Both atoms do this in order to have 8 valence electrons.
Compounds held together by ionic bonds are called salts.
Unit 1 Student Notes Page 27
Table of Contents Link
Ionic Bonds are very strong when the compound is dry.
Ionic bonds are easily broken in water. This is why many salts dissolve easily in water to form
ions.
Cations – Ions which possess a positive charge because they have more protons than
electrons. The metal atoms in a salt typically become cations.
Anions –Ions which possess a negative charge because they have more electrons than
protons. The non-metal atoms in a salt typically become anions.
Hydrogen Bonds
Hydrogen Bonds are fairly weak (compared to covalent and ionic bonds) intermolecular attractions
that occur between polar molecules. They are often depicted as dots in chemical diagrams.
Hydrogen bonding is very important in water due to its polar nature.
AP Biology
Biochemistry of Water
AP Biology
Biochemistry: Carbon Properties
Organic Chemistry
Branch of science dealing with the element carbon and its many properties.
Most of the compounds found in living things, other than water, are organic.
About 30% of an organism’s dry weight (Biomass) is composed of Carbon found in the body’s organic
molecules.
Carbon helps to make the 4 major groups of organic macromolecules: Carbohydrates, Lipids, Proteins, and
Nucleic Acids.
The original source for Carbon in all life forms is Carbon Dioxide. (CO2 - Photosynthesis)
Organic Macromolecules
Polymers
These are large molecules that are formed by combining/bonding individual units called
monomers.
The monomers are linked together by covalent bonds. Remember that covalent bonds are strong.
Macromolecules are broken apart into individual monomers by Hydrolysis reactions. (“lysis” means “to
split.”). In these reactions, water is used as a reactant.
Carbohydrates
Carbohydrates are sugars. In living things, carbohydrates serve as sources of quick energy and as
structural/building materials. Most carbohydrate names end in the letters “-ose”.
Monosaccharides - Are the monomers or “building blocks” of carbohydrates. (“sacch” means “sugar”.)
Glucose, fructose, galactose, ribose, and deoxyribose are common monosaccharides. The general
molecular formula for a monosaccharide is (CNH2NON).
Polysaccharides - Are the polymers. These compounds are formed by the bonding together of several
monosaccharides. Biologically important polysaccharides include:
Although starch, cellulose, and glycogen are all polymers of glucose, the molecules have different
shapes. Some of these complex carbohydrates consist of straight chains of monomers, while others
consist of branched chains. Because of the orientation of the glucose monomers, many hydrogen
bonds form in cellulose and cause the molecule to be very strong and hard to digest, while starch is
relatively easy to digest.
Unit 1 Student Notes Page 32
Table of Contents Link
Lipids
These macromolecules are fats, oils, waxes, and steroids.
Most lipids are hydrophobic molecules. They contain little oxygen and are mostly nonpolar in nature.
Two Main parts of a lipid:
Fatty Acid—long chain of carbon and hydrogen atoms.
3 Carbon Glycerol molecule (alcohol) to hold the whole molecule together.
Lipids use a covalent bond called an Ester Linkage to hold the fatty acids and glycerol together.
Unsaturated fats--These fatty acid chains contain some carbon-carbon double or triple
bonds that “could be broken” to add more Hydrogen to the fatty acid. Saturated fats tend to
be liquids at room temperature and they usually are associated with plants (vegetable oil,
sunflower oil, or peanut oil). Unsaturated fats are typically viewed as a healthy part of the
diet.
Polyunsaturated fats--These fats have many double or triple bonds in their fatty acid chains.
Hydrogenated or Trans fats. These are oils turned solid fats by adding Hydrogen and by
breaking the double or triple bonds in the fatty acids. This was done in the past to change the
texture, stability, and shelf life of fats. Trans fats were common in processed foods. They
have been shown to increase LDL cholesterol levels and to contribute to coronary artery
disease.
Unit 1 Student Notes Page 33
Table of Contents Link
Phospholipids
These molecules replace a single fatty acid chain from a triglyceride with a single Phosphate
ion. The phosphate portion of the molecule is Hydrophilic because of the charge on the
phosphate ion.
The remaining fatty acids chains are hydrophobic. They are mostly composed of long chains
of carbon atoms that are also bonded to hydrogens. They are neutral and are not attracted to
water.
Phospholipids are said to be amphipathic since they have both polar and nonpolar sides.
Phospholipid Bi-layers are important for the building of cell and organelle membranes.
Steroids
A steroid is a lipid composed of 4 carbon rings. Common steroids found in the body include
testosterone, estrogen, progesterone, and cholesterol.
What makes them different from each other are the attached functional groups. These
functional groups help determine the function of the steroid. Most of the steroids are built
from cholesterol. Steroids function in the body as cell signals/hormones. Due to their
lipid/nonpolar nature they can penetrate the cell membrane and bind to intracellular receptors.
They often act to regulate the expression of certain genes.
Unit 1 Student Notes Page 34
Table of Contents Link
Cholesterol is an important component of the cell membrane. It helps with cell membrane
flexibility.
Common Steroids
Proteins
Proteins make up greater than 50% of an organism’s dry weight or biomass.
The names of most proteins end in “lin” while the names of most enzymes (which are composed of proteins)
usually end in “ase”.
Proteins are large macromolecules which are composed of monomers “building blocks” called Amino Acids.
There are 20 different Amino Acids used by living things to make proteins. Proteins and enzymes usually have
hundreds to thousands of Amino acids in their structure.
Individual Amino Acids (monomers) are bonded together by a covalent bond called a peptide bond. The peptide
bond is a covalent bond and is strong and hard to break.
In order to create a peptide bond, the amino end of one amino acid is positioned to combine with the Carboxyl
end of the second amino acid. The amino acids are joined during dehydration synthesis reactions (also known as
“condensation reactions”).
Two amino acids bonded together are referred to as a dipeptide. When more than two are bonded, the structure is
referred to as a polypeptide chain.
Unit 1 Student Notes Page 36
Table of Contents Link
Because of the structure of the amino acids, a polypeptide chain has directionality, meaning that it has two ends
that are chemically distinct from one another. At one end, the polypeptide has a free amino group, and this end is
called the amino terminus (or N-terminus). The other end, which has a free carboxyl group, is known as
the carboxyl terminus (or C-terminus). The N-terminus is on the left and the C-terminus is on the right for the
very short polypeptide shown above.
New amino acids are always added to the carboxyl terminus of a growing polypeptide chain.
A protein is typically made from several polypeptide chains that are wrapped together into a large 3-D unit.
The information included below discusses the four levels of protein structure.
For proteins that are built by ribosomes located on the rough ER, this folding takes place within the Rough
Endoplasmic Reticulum. These proteins are usually exported from the cell through the process of
exocytosis (secretion).
Other proteins are constructed by ribosomes which float freely in the cytosol. These proteins typically
remain within the cell in which they were made. The folding of these proteins usually takes place within a
chaperonin. Chaperonins are protective structures that allows proteins to fold without water present.
Unit 1 Student Notes Page 37
Table of Contents Link
Two common types of secondary structure are the alpha helix and the beta pleated sheet.
The tertiary structure is also partially determined by ionic interactions between certain “R” groups and by
hydrophobic interactions between certain R groups and water.
Unit 1 Student Notes Page 38
Table of Contents Link
Denaturation
The “unraveling” or “unfolding” of a protein or enzyme causing it not to function.
Denaturation can be caused by pH changes, salt concentration changes, and increases in temperature.
Denaturation usually disrupts the secondary and tertiary levels of protein structure by affecting either
the hydrogen bonds or disulfide bonds which stabilize the structure.
Nitrogen Cycle
Although there is plenty of nitrogen found in the air, the amount of usable nitrogen available for life on Earth
is limited. Since the nitrogen atoms in nitrogen gas are held together by triple covalent bonds, atmospheric
nitrogen is difficult for life forms to break apart and use. The nitrogen cycle is the process via which nitrogen
moves from the atmosphere into living things and ultimately back to the atmosphere. Cycles like the nitrogen
cycle, the carbon cycle, the water cycle, and the phosphorus cycle are collectively known as the biogeochemical
cycles. These processes continuously cycle elements throughout the Earth.
Nitrogen is an essential element for the construction of proteins and amino acids. Nitrogen is also an important
component of nucleic acids such as DNA, RNA, and ATP. Some nitrogen is removed from the air by rainwater.
Remember, water is the universal solvent, so the gas is dissolved in the rain. The Nitrogen in the water can be
consumed by Nitrogen Fixing bacteria, in the soil, that convert it into Ammonium ions (NH4+). This process is
referred to as Nitrogen Fixation. The Ammonium ions can then be absorbed by plants to help make proteins and
DNA or RNA. Some Ammonium in the soil is also consumed by Nitrifying Bacteria, and converted to Nitrite (NO2-)
first and then ultimately into Nitrate (NO3-). This process is called Nitrification. The Nitrates are also
absorbed by the plants, just as was the Ammonium ions. Other bacteria, called denitrifying bacteria, in the soil can
Unit 1 Student Notes Page 40
Table of Contents Link
also absorb the nitrates and convert them back into Oxygen gas (O2) and Nitrogen gas (N2). These molecules
are both returned to the air to be used again. This process is called Denitrification. As plants are eaten by
animals, the Nitrogen travels through the food chain. When all life forms die, the bodies decompose and
create Ammonia (NH3), which is why they stink. The Ammonia is converted by bacteria into
Ammonium to be used again by plants and bacteria. This conversion is called
Ammonification. Some Nitrogen is also released by animals in their urine. It too undergoes
Ammonification.
Nucleic Acids
Nucleic Acids function to store genetic information and/or to store and transfer energy. Common nucleic
acids found living organisms include: DNA, RNA, ATP, cAMP, NADH, and NADPH.
The monomers of nucleic acids are called nucleotides. A nucleotide consists of a 5 carbon (pentose) sugar
bonded to a phosphate group and a nitrogenous base.
Unit 1 Student Notes Page 41
Table of Contents Link
DNA and mRNA are both polymers. DNA and RNA are the primary sources of genes and hereditary
information.
1. DNA has Deoxyribose as its 5 Carbon sugar. DNA is double stranded. In eukaryotic cells, DNA is
always stored inside a nuclear membrane or envelope. DNA’s function is to code for proteins.
The sequence of the nitrogenous bases in the DNA determines the order of the amino acids in each
of the body’s proteins.
Watson and Crick were eventually able to determine that the DNA molecule is composed of two strands of
nucleotides that are then twisted into a double helix. The individual strands are built when the phosphate groups
of the nucleotides form covalent bonds with the deoxyribose molecules of adjacent nucleotides. The actual bonds
form when one deoxyribose attaches to another by connecting its 5' carbon to the 3' carbon of the next sugar in the
next nucleotide using a phosphate group. The alternating sugars and phosphates form the “backbone” of the DNA
molecule.
The two strands are connected together by hydrogen bonding between complementary nitrogenous bases. An A on
one strand bonds with a T on the other strand. A G on one strand binds with a C on the other strand. Each A-T base
pair is held together by 2 hydrogen bonds, while each G-C pair is held together by 3 hydrogen bonds. This
means that it is easier to separate DNA strands with lots of A-T base pairs than it is to separate strands with
lots of G-C base pairs. It is important to remember that hydrogen bonds are weak when compared to covalent or
ionic bonds. This is important, because the two DNA strands have to be separated during both the processes of
replication and transcription.
Like a protein, a DNA molecule has directionality. The DNA molecule is composed of two strands of
nucleotides held together by hydrogen bonds. Each strand has two slightly different ends. One end, known as the 5’
end, terminates with an unbound 5’ carbon on the last nucleotide in the chain. The other end, known as the 3’ end,
terminates with an unbound 3’ carbon on the last deoxyribose molecule at its end. When the two strands are
connected together, they are oriented in opposite directions. Because they run parallel to each other, but have
opposite directional orientations, the two strands are said to be antiparallel.
Unit 1 Student Notes Page 42
Table of Contents Link
2. RNA has Ribose as its 5 Carbon sugar. RNA is single stranded. There are several types of RNA.
Messenger RNA (mRNA) is made from the DNA template during the process of transcription.
mRNA’s job is to transmit the protein building directions from the DNA in the nucleus to the
ribosomes in the cytoplasm. Transfer RNA’s (tRNA) job is to deliver and place the appropriate
amino acids into the proteins that are built by the ribosomes. Ribosomal RNA (rRNA) is one of the
main building components of the cell’s ribosomes.
Unit 1 Student Notes Page 43
Table of Contents Link
Scientists can now sequence the nucleotide/nitrogenous bases found in genes of an organism and compare this sequence to
the sequence of the same gene found in another organism. The more similar the two sequences are, the more related the
two organisms are.
ATP (Adenosine Triphosphate) is another important nucleic acid. An ATP molecule is composed of a single nucleotide
which consists of the sugar (ribose) bonded to a nitrogenous base (always adenine), and three phosphate groups. ATP’s
role in the body is to store and transfer energy. ATP is made during the process of cellular respiration. It functions to
power almost every activity that occurs in the cell.
Phosphorus Cycle
The phosphorus cycle is another important biogeochemical cycle. Phosphorus is an important component of
DNA, RNA, ATP, phospholipids, and bone. Most of the Earth’s phosphorus is found in rock. As the rock
weathers, some of the phosphorus is released into the soil. Some dissolves into the water as the rains pass through
the soil. This phosphorus makes its way into bodies of water and is available for producers (phytoplankton) to use
to make organic compounds such as phospholipids, DNA, RNA, ATP, etc... Plants can also retrieve the
Unit 1 Student Notes Page 44
Table of Contents Link
phosphorus directly from the soil and use it to make organic compounds. When organisms die, decomposers
break down the bodies and return the phosphorus to the soil so that it can be reused.