Unit Test — Unit test Answers

25 verified answers
3

Which is composed of alkenes?

A
welding torch fuel
B
polystyrene cups
C
propane gas
D
degreaser containing hexane
4

What is a disadvantage of using a space-filling model to show a chemical compound?

A
Space-filling models provide a two-dimensional view of the molecule.
B
Space-filling models do not identify the number and type of bonds.
C
Space-filling models do not show all atoms in the molecule.
D
Space-filling models show information about composition but not structure.
5

Which compound can be used to preserve biological specimens?

A
A central C is double bonded to an O, and single bonded to 2 H.
Option A
B
A chain, reading from left: C H 3 bonded to C, bonded to O, bonded to C H 2, bonded to C H2, bonded to C H 3. The single C near the beginning of the chain is double bonded to O.
Option B
C
C H 3 single bonded to C, which is double bonded above right to O, and below right to C H 2, which is bonded to C H 3.
Option C
D
A central C is double bonded to an O above, and single bonded to C H 3 below left and O H below right.
Option D
6

What are geometric isomers?

A
compounds that have the same types of atoms arranged in different orders
B
compounds that have the same number of carbon atoms arranged in different orders
C
compounds that have the same atoms arranged in the same order, but with different three-dimensional orientations
D
compounds that have the same atoms arranged in the same order, and have the same three-dimensional orientations
10

What is the name of this hydrocarbon?

Question illustration
A
1-methylbutane
B
2-methylbutane
C
2-methylpropane
D
3-methylpropane
13

Which activity most likely involves the direct use of saturated hydrocarbons?

A
burning natural gas
B
dissolving salt in water
C
carving stone with hammer and chisel
D
bending steel by hand
14

The molecular formula for methanol is CH3OH. Which model shows methanol? (black = carbon; red = oxygen; white = hydrogen)

A
mc022-1.jpg
Option A
B
A space-filling model has a black atom with three white atoms bonded to a red atom with one white atom.
Option B
C
A ball and stick model has 2 black atoms bonded to each other. One has three white atoms bonded to it; the other has two white atoms, and a red atom bonded to a white atom.
Option C
D
A central red atom is bonded on each side to a black atom, each of which is bonded to 3 white atoms.
Option D
15

Consider this hydrocarbon.Is this an aromatic hydrocarbon? Why or why not?

Question illustration
A
Yes, because the carbon chain is made up of single bonds.
B
Yes, because the carbon chain is ring shaped.
C
No, because the carbon chain is composed of only a single ring.
D
No, because the carbon chain has no double bonds.
17

Which is a property of both alkenes and alkynes?

A
Both are highly water soluble.
B
The pH of these hydrocarbons tends to be very basic.
C
Their boiling points tend to increase with chain length.
D
Their densities are all much higher than that of water.
19

How does a straight-chain alkane that has five carbon atoms differ from a cycloalkane that has five carbon atoms?

A
The straight-chain alkane has at least one double or triple bond, but the cycloalkane has only single bonds.
B
The straight-chain alkane has only single bonds, but the cycloalkane has at least one double or triple bond.
C
The straight-chain alkane has two more hydrogen atoms than the cycloalkane.
D
The straight-chain alkane has two fewer hydrogen atoms than the cycloalkane.
20

The compound butanol has the following structural formula.Which of these is a structural isomer of butanol?

Question illustration
A
A string of 4 C atoms are bonded above, below, left and right to H.
B
A string of 4 C atoms is bonded above, below, left, and right to H, except the second C, which is bonded below to O, which is bonded below to H.
C
A string of 4 C atoms is bonded above, below, left, and right to H, but the chain is interrupted between the first and second C, which are bonded to an O between them.
D
A string of 4 C atoms is bonded above, below, and left to H, except the last C has no H below and is double-bonded to an O to the right.

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