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5.5.1 Practice
5.5.1 Practice
5.5.1 Practice
25 points)
Complete the table by labeling each molecule an alkane, alkene, or alkyne. (2.25 points total)
Pentane Alkane
Alkyne
Alkane
Alkyne
Octene Alkene
Alkane
Alkane
Butyne Alkyne
Alkene
A. Write the name of the alkane next to the drawing of the molecule. (2.25 points)
Heptane
Octane
Propane
Methane
Propane
Ethane
Pentane
Butane
Hexane
B. Write the name of the alkene next to the drawing of the molecule. Names include: 1-pentene,
Cis-2-butene
Trans-2-butene
1-propene
cis-2-pentene
1-pentene
trans-pentene
C. Write the name of the alkyne next to the drawing of the molecule. (1.5 points)
D. Write the name of the branched alkane next to the drawing of the molecule. (1.5 points)
3-methylheptane
2-methylpentane
2-methylheptane
3-methylpentane
2-methylhexane
3-methylhexane
Question 3: Functional Groups (7 points)
Carboxylic acid
Ether
Ester
Aldehyde
Ketone
Amine
Alcohol
B. Identify the type of molecule from the name of the molecule. (3.5 points)
Hexanol Alcohol
Octanal Aldehyde
Benzophenone Ketone
Chlorpheniramine Amine
Read pages 1 – 5 of the practice activity to find information that will help you answer question
4.
It would most likely interact with the side containing the OH group.
ii. Why would you expect a long alcohol molecule to be insoluble in water and a small
Longer chains are most likely less soluble because there is less interaction with the
solvent. Water only reacts with the OH section of the molecule, while the rest is nonpolar.
B. Rank the boiling points of methane, methanol, and methanal from lowest to highest. Explain
C. The lone pair of electrons on the oxygen atom in an ester can form hydrogen bonds in some
situations, but esters cannot form hydrogen bonds with each other. How would you expect the
Esters would likely have a lower boiling point. This is because esters cannot form
hydrogen bonds due to there being no free hydrogen atoms, which would raise the boiling point
significantly, while alcohols can.
D. Can an ether form hydrogen bonds in the same way an ester does? Why or why not? (1 point)
They both act similarly. An ether acts like a HBA and accepts hydrogen bonds, just like
esters. However, ethers have an open space to bind with other molecules.
E. What would be the product of this reaction? Draw the molecule and name it. (1 point)
Propene + Water Propanol
F. What type of molecule is produced when butanoic acid reacts with methanol? (1 point)
An ester
G. Aldehydes form from the oxidation of alcohols. If you add water to an aldehyde, you get this
What type of molecule do you get if you oxidize an aldehyde hydrate? Hint: Do the same thing to
A carboxylic acid.
Question 5: Biological Molecules (4 points)
glucose to fructose. What effect does this enzyme have on this reaction? (1 point)
The enzyme would likely reduce the necessary activation energy, while also speeding up
the procedure.
B. Why would using this enzyme be beneficial for someone who wants to produce a large
Nucleic acids are used in DNA, which gives cells instructions. RNA is then created, which
creates proteins.
D. Why can damage to a nucleic acid lead to a person not producing an enzyme? (1 point)
types of fatty acids listed in nutrition labels on foods. Based on what you have learned about
fatty acids, bonding, and naming of chemical compounds, see if you can make an educated
guess as to what the chemical structures of the following fatty acids are. (1 point each)
A. Monounsaturated fatty acids: Think about what unsaturated fats contain, and what number is
B. Polyunsaturated fatty acids: Think about what the prefix poly- means in the terms polypeptide
and polymer.
Most likely an alkene. It cannot rotate, and has groups attached to the carbon atoms of
the double bond that are fixed relative to each other.
A. Sort the types of energy into the "renewable" and "nonrenewable" columns. (2 points)
Energy types: Coal, Petroleum, Solar, Wind, Hydroelectric, Geothermal, Biomass, Natural Gas
Renewable Nonrenewable
Solar Coal
Wind Petroleum
Hydroelectric Natural Gas
Geothermal
Biomass
D. What is a disadvantage of using biomass that the other types of alternative fuels do not
have? (1 point)
Biomass is better because it is renewable and the material biomass is made for would
take up valuable space if not used. Oil and coal are nonrenewable and are buried deep in areas
where it would not impact anyone.
F. What advantage does nuclear power have over solar, wind, and hydroelectric? (1 point)