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Organic Chemistry

John McMurry

Chapter 7

Alkenes: Structure and Reactivity - all with Video Answers

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Chapter Questions

02:37

Problem 1

Calculate the degree of unsaturation in each of the following formulas, and then draw as many structures as you can for each:
(a) $\mathrm{C}_{4} \mathrm{H}_{8}$
(b) $\mathrm{C}_{4} \mathrm{H}_{6}$
(c) $\mathrm{C}_{3} \mathrm{H}_{4}$

Grigoriy Sereda
Grigoriy Sereda
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07:54

Problem 2

Calculate the degree of unsaturation in each of the following formulas:
(a) $\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{~N}$
(b) $\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{NO}_{2}$
(c) $\mathrm{C}_{8} \mathrm{H}_{9} \mathrm{Cl}_{3}$
(d) $\mathrm{C}_{9} \mathrm{H}_{16} \mathrm{Br}_{2}$
(e) $\mathrm{C}_{10} \mathrm{H}_{12} \mathrm{~N}_{2} \mathrm{O}_{3}$
(f) $\mathrm{C}_{20} \mathrm{H}_{32} \mathrm{ClN}$

Shalini Tyagi
Shalini Tyagi
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02:51

Problem 3

Diazepam, marketed as an antianxiety medication under the name Valium, has three rings, eight double bonds, and the formula $\mathrm{C}_{16} \mathrm{H}_{?} \mathrm{ClN}_{2} \mathrm{O} .$ How many hydrogens does diazepam have? (Calculate the answer; don't count hydrogens in the structure.)

Lijeesh Krishnan
Lijeesh Krishnan
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10:31

Problem 4

Give IUPAC names for the following compounds:

Ricajoy Montero
Ricajoy Montero
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04:11

Problem 5

Draw structures corresponding to the following IUPAC names:
(a) 2 -Methyl-1,5-hexadiene
(b) 3 -Ethyl-2,2-dimethyl-3-heptene
(c) 2,3,3 -Trimethyl-1,4,6-octatriene
(d) 3,4 -Diisopropyl-2,5-dimethyl-3-hexene

Lijeesh Krishnan
Lijeesh Krishnan
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02:36

Problem 6

Name the following cycloalkenes:

Grigoriy Sereda
Grigoriy Sereda
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02:53

Problem 7

Change the following old names to new, post-1993 names, and draw the structure of each compound:
(a) 2,5,5 -Trimethyl-2-hexene
(b) 2,3 -Dimethyl-1,3-cyclohexadiene

Grigoriy Sereda
Grigoriy Sereda
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01:54

Problem 8

The sex attractant of the common housefly is an alkene named $c i s-9$ -tricosene. Draw its structure. (Tricosane is the straight-chain alkane $\mathrm{C}_{23} \mathrm{H}_{48}$.)

Lijeesh Krishnan
Lijeesh Krishnan
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06:41

Problem 9

Which of the following compounds can exist as pairs of cis-trans isomers? Draw each cis-trans pair, and indicate the geometry of each isomer.
(a) $\mathrm{CH}_{3} \mathrm{CH}=\mathrm{CH}_{2}$
(b) $\left(\mathrm{CH}_{3}\right)_{2} \mathrm{C}=\mathrm{CHCH}_{3}$
(c) $\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{CH}=\mathrm{CHCH}_{3}$
(d) $\left(\mathrm{CH}_{3}\right)_{2} \mathrm{C}=\mathrm{C}\left(\mathrm{CH}_{3}\right) \mathrm{CH}_{2} \mathrm{CH}_{3}$
(e) $\mathrm{ClCH}=\mathrm{CHCl}$
(f) $\mathrm{BrCH}=\mathrm{CHCl}$

Shalini Tyagi
Shalini Tyagi
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02:01

Problem 10

Name the following alkenes, including a cis or trans designation:

Grigoriy Sereda
Grigoriy Sereda
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01:53

Problem 11

Which member in each of the following sets ranks higher?
(a) $-\mathrm{H}$ or $-\mathrm{CH}_{3}$
(b) $-\mathrm{Cl}$ or $-\mathrm{CH}_{2} \mathrm{Cl}$
(c) $-\mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{Br}$ or $-\mathrm{CH}=\mathrm{CH}_{2}$
(d) $-\mathrm{NHCH}_{3}$ or $-\mathrm{OCH}_{3}$
(e) $-\mathrm{CH}_{2} \mathrm{OH}$ or $-\mathrm{CH}=\mathrm{O}$
(f) $-\mathrm{CH}_{2} \mathrm{OCH}_{3}$ or $-\mathrm{CH}=\mathrm{O}$

Grigoriy Sereda
Grigoriy Sereda
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11:40

Problem 12

Rank the substituents in each of the following sets according to the sequence rules:
(a) $-\mathrm{CH}_{3},-\mathrm{OH},-\mathrm{H},-\mathrm{Cl}$
(b) $-\mathrm{CH}_{3},-\mathrm{CH}_{2} \mathrm{CH}_{3},-\mathrm{CH}=\mathrm{CH}_{2},-\mathrm{CH}_{2} \mathrm{OH}$
(c) $-\mathrm{CO}_{2} \mathrm{H},-\mathrm{CH}_{2} \mathrm{OH},-\mathrm{C} \equiv \mathrm{N},-\mathrm{CH}_{2} \mathrm{NH}_{2}$
(d) $-\mathrm{CH}_{2} \mathrm{CH}_{3},-\mathrm{C} \equiv \mathrm{CH},-\mathrm{C} \equiv \mathrm{N},-\mathrm{CH}_{2} \mathrm{OCH}_{3}$

Shalini Tyagi
Shalini Tyagi
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02:49

Problem 13

Assign $E$ or $Z$ configuration to the following alkenes:

Susan Hallstrom
Susan Hallstrom
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01:37

Problem 14

Assign stereochemistry $(E$ or $Z$ ) to the double bond in the following compound, and convert the drawing into a skeletal structure (red $=\mathrm{O}$ ):

Grigoriy Sereda
Grigoriy Sereda
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01:56

Problem 15

Name the following alkenes, and tell which compound in each pair is more stable:

Grigoriy Sereda
Grigoriy Sereda
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02:05

Problem 16

Predict the products of the following reactions:

Grigoriy Sereda
Grigoriy Sereda
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02:30

Problem 17

What alkenes would you start with to prepare the following products?

Grigoriy Sereda
Grigoriy Sereda
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01:11

Problem 18

Show the structures of the carbocation intermediates you would expect in the following reactions:

Grigoriy Sereda
Grigoriy Sereda
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01:18

Problem 19

Draw a skeletal structure of the following carbocation. Identify it as primary, secondary, or tertiary, and identify the hydrogen atoms that have the proper orientation for hyperconjugation in the conformation shown.

Grigoriy Sereda
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Problem 20

What about the second step in the electrophilic addition of HCl to an alkenethe reaction of chloride ion with the carbocation intermediate? Is this step exergonic or endergonic? Does the transition state for this second step resemble the reactant (carbocation) or product (alkyl chloride)? Make a rough drawing of what the transition-state structure might look like.

Lainey Roebuck
Lainey Roebuck
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05:21

Problem 21

On treatment with HBr, vinylcyclohexane undergoes addition and rearrangement to yield 1-bromo-1-ethylcyclohexane. Using curved arrows, propose a mechanism to account for this result.

Shalini Tyagi
Shalini Tyagi
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01:38

Problem 22

Name the following alkenes, and convert each drawing into a skeletal structure:

Grigoriy Sereda
Grigoriy Sereda
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01:57

Problem 23

Assign $E$ or $Z$ stereochemistry to the double bonds in each of the following alkenes, and convert each drawing into a skeletal structure (red $=\mathrm{O},$ green $=\mathrm{Cl}$ )

Grigoriy Sereda
Grigoriy Sereda
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01:35

Problem 24

The following carbocation is an intermediate in the electrophilic addition reaction of HCl with two different alkenes. Identify both, and tell which $\mathrm{C}-\mathrm{H}$ bonds in the carbocation are aligned for hyperconjugation with the vacant $p$ orbital on the positively charged carbon.

Grigoriy Sereda
Grigoriy Sereda
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00:43

Problem 25

The following alkyl bromide can be made by HBr addition to three different alkenes. Show their structures.

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Problem 26

Predict the major product and show the complete mechanism for each electrophilic reaction below.

Lainey Roebuck
Lainey Roebuck
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03:03

Problem 27

Each electrophilic addition reaction below involves a carbocation rearrangement. Predict the product and draw the complete arrow-pushing mechanism.

Nicole Krahulik
Nicole Krahulik
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08:03

Problem 28

When 1,3 -butadiene reacts with one mole of HBr, two isolable products result. Propose a mechanism to explain this.

Shalini Tyagi
Shalini Tyagi
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01:39

Problem 29

When methyl vinyl ether reacts with a strong acid, the proton adds to C2 exclusively, instead of C 1 or the oxygen atom. Draw the three protonated forms of methyl vinyl ether and explain this observation.

Anand Jangid
Anand Jangid
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01:30

Problem 30

Addition of HCl to 1 -isopropylcyclohexene yields a rearranged product. Propose a mechanism, showing the structures of the intermediates and using curved arrows to indicate electron flow in each step.

Grigoriy Sereda
Grigoriy Sereda
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07:15

Problem 31

Addition of $\mathrm{HCl}$ to 1 -isopropenyl-1-methylcyclopentane yields 1 -chloro- 1,2,2 -trimethylcyclohexane. Propose a mechanism, showing the structures of the intermediates and using curved arrows to indicate electron flow in each step.

Shalini Tyagi
Shalini Tyagi
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01:27

Problem 32

Addition of HCl to 1 -isopropenyl-1-methylcyclopentane yields 1 -chloro-1,2,2-trimethylcyclohexane. Propose a mechanism, showing the structures of the intermediates and using curved arrows to indicate electron flow in each step.

Ronald Prasad
Ronald Prasad
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10:04

Problem 33

epi-Aristolochene, a hydrocarbon found in both pepper and tobacco, is biosynthesized by the following pathway. Add curved arrows to show the mechanism of each step. Which steps involve alkene electrophilic addition(s), and which involve carbocation rearrangement(s)? (The abbreviation H-A stands for an unspecified acid, and "Base" is an unspecified base in the enzyme.)

Dr.  Satish  Ingale
Dr. Satish Ingale
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02:55

Problem 34

Calculate the degree of unsaturation in the following formulas, and draw five possible structures for each:
(a) $\mathrm{C}_{10} \mathrm{H}_{16}$
(b) $\mathrm{C}_{8} \mathrm{H}_{8} \mathrm{O}$
(c) $\mathrm{C}_{7} \mathrm{H}_{10} \mathrm{Cl}_{2}$
(d) $\mathrm{C}_{10} \mathrm{H}_{16} \mathrm{O}_{2}$
(e) $\mathrm{C}_{5} \mathrm{H}_{9} \mathrm{NO}_{2}$
(f) $\mathrm{C}_{8} \mathrm{H}_{10} \mathrm{ClNO}$

Anand Jangid
Anand Jangid
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01:53

Problem 35

How many hydrogens does each of the following compounds have?
(a) $\mathrm{C}_{8} \mathrm{H}_{?} \mathrm{O}_{2}$, has two rings and one double bond
(b) $\mathrm{C}_{7} \mathrm{H}_{?} \mathrm{~N}$, has two double bonds
(c) $\mathrm{C}_{9} \mathrm{H}_{?} \mathrm{NO}$, has one ring and three double bonds

Anand Jangid
Anand Jangid
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00:59

Problem 36

Loratadine, marketed as an antiallergy medication under the name Claritin, has four rings, eight double bonds, and the formula $\mathrm{C}_{22} \mathrm{H}_{2} \mathrm{ClN}_{2} \mathrm{O}_{2}$. How many hydrogens does loratadine have? (Calculate your answer; don't count hydrogens in the structure.)

Grigoriy Sereda
Grigoriy Sereda
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03:54

Problem 37

Name the following alkenes:

Grigoriy Sereda
Grigoriy Sereda
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02:39

Problem 38

Draw structures corresponding to the following systematic names:
(a) $(4 E)-2,4$ -Dimethyl-1,4-hexadiene
(b) $c i s-3,3$ -Dimethyl- 4 -propyl-1,5-octadiene
(c) 4 -Methyl-1,2-pentadiene
(d) $(3 E, 5 Z)-2,6$ -Dimethy $1-1,3,5,7$ -octatetraene
(e) 3 -Butyl-2-heptene
(f) trans-2,2,5,5-Tetramethyl-3-hexene

Anand Jangid
Anand Jangid
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02:36

Problem 39

Name the following cycloalkenes:

Grigoriy Sereda
Grigoriy Sereda
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01:22

Problem 40

Ocimene is a triene found in the essential oils of many plants. What is its IUPAC name, including stereochemistry?

Grigoriy Sereda
Grigoriy Sereda
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01:31

Problem 41

$\alpha$ -Farnesene is a constituent of the natural wax found on apples. What is its IUPAC name, including stereochemistry?

Grigoriy Sereda
Grigoriy Sereda
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00:38

Problem 42

Menthene, a hydrocarbon found in mint plants, has the systematic name 1 -isopropyl-4-methylcyclohexene. Draw its structure.

Grigoriy Sereda
Grigoriy Sereda
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01:37

Problem 43

Draw and name the six alkene isomers, $\mathrm{C}_{5} \mathrm{H}_{10}$, including $E, Z$ isomers.

Grigoriy Sereda
Grigoriy Sereda
Numerade Educator
02:24

Problem 44

Draw and name the 17 alkene isomers, $\mathrm{C}_{6} \mathrm{H}_{12}$, including $E, Z$ isomers.

Grigoriy Sereda
Grigoriy Sereda
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Problem 45

Rank the following sets of substituents according to the Cahn-IngoldPrelog sequence rules:
(a) $-\mathrm{CH}_{3},-\mathrm{Br},-\mathrm{H},-\mathrm{I}$
(b) $-\mathrm{OH},-\mathrm{OCH}_{3},-\mathrm{H},-\mathrm{CO}_{2} \mathrm{H}$
(c) $-\mathrm{CO}_{2} \mathrm{H},-\mathrm{CO}_{2} \mathrm{CH}_{3},-\mathrm{CH}_{2} \mathrm{OH},-\mathrm{CH}_{3}$
(d) $-\mathrm{CH}_{3},-\mathrm{CH}_{2} \mathrm{CH}_{3},-\mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{OH},-\stackrel{\|}{\mathrm{CCH}_{3}}$
(e) $-\mathrm{CH}=\mathrm{CH}_{2},-\mathrm{CN},-\mathrm{CH}_{2} \mathrm{NH}_{2},-\mathrm{CH}_{2} \mathrm{Br}$
(f) $-\mathrm{CH}=\mathrm{CH}_{2},-\mathrm{CH}_{2} \mathrm{CH}_{3},-\mathrm{CH}_{2} \mathrm{OCH}_{3},-\mathrm{CH}_{2} \mathrm{OH}$

Lainey Roebuck
Lainey Roebuck
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02:43

Problem 46

Assign $E$ or $Z$ configuration to each of the following compounds:

Grigoriy Sereda
Grigoriy Sereda
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03:27

Problem 47

Which of the following $E, Z$ designations are correct, and which are incorrect?

Grigoriy Sereda
Grigoriy Sereda
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Problem 48

Rank the double bonds below in terms of increasing stability.

Lainey Roebuck
Lainey Roebuck
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00:58

Problem 49

trans-2-Butene is more stable than cis-2-butene by only $4 \mathrm{~kJ} / \mathrm{mol}$, but trans-2,2,5,5-tetramethyl-3-hexene is more stable than its cis isomer by $39 \mathrm{~kJ} / \mathrm{mol} .$ Explain.

Grigoriy Sereda
Grigoriy Sereda
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00:51

Problem 50

Cyclodecene can exist in both cis and trans forms, but cyclohexene cannot. Explain. (Making molecular models is helpful.)

Grigoriy Sereda
Grigoriy Sereda
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05:39

Problem 51

Normally, a trans alkene is more stable than its cis isomer. transCyclooctene, however, is less stable than $c i s$ -cyclooctene by $38.5 \mathrm{~kJ} /$ mol. Explain.

Shalini Tyagi
Shalini Tyagi
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08:37

Problem 52

trans-Cyclooctene is less stable than cis-cyclooctene by $38.5 \mathrm{~kJ} / \mathrm{mol}$, but trans-cyclononene is less stable than cis-cyclononene by only $12.2 \mathrm{~kJ} / \mathrm{mol} .$ Explain.

Shalini Tyagi
Shalini Tyagi
Numerade Educator
01:35

Problem 53

Tamoxifen, a drug used in the treatment of breast cancer, and clomiphene, a drug used in fertility treatment, have similar structures but very different effects. Assign $E$ or $Z$ configuration to the double bonds in both compounds.

Grigoriy Sereda
Grigoriy Sereda
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Problem 54

Rank the carbocations below in terms of increasing stability.

Lainey Roebuck
Lainey Roebuck
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Problem 55

Use Hammond's Postulate to determine which alkene in each pair would be expected to form a carbocation faster in an electrophilic addition reaction.

Lainey Roebuck
Lainey Roebuck
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01:35

Problem 56

Carbocations can be stabilized by resonance. Draw all the resonance forms that would stabilize each carbocation.

Anand Jangid
Anand Jangid
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05:04

Problem 57

Predict the major product in each of the following reactions:

Susan Hallstrom
Susan Hallstrom
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01:45

Problem 58

Predict the major product from addition of $\mathrm{HBr}$ to each of the following alkenes:

Grigoriy Sereda
Grigoriy Sereda
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01:34

Problem 59

Alkenes can be converted into alcohols by acid-catalyzed addition of water. Assuming that Markovnikov's rule is valid, predict the major alcohol product from each of the following alkenes.

Grigoriy Sereda
Grigoriy Sereda
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01:33

Problem 60

Each of the following carbocations can rearrange to a more stable ion. Propose structures for the likely rearrangement products.

Nicole Krahulik
Nicole Krahulik
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03:53

Problem 61

Allene (1,2-propadiene), $\mathrm{H}_{2} \mathrm{C}=\mathrm{C}=\mathrm{CH}_{2}$, has two adjacent double bonds. What kind of hybridization must the central carbon have? Sketch the bonding $\pi$ orbitals in allene. What shape do you predict for allene?

Ronald Prasad
Ronald Prasad
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Problem 62

The heat of hydrogenation for allene (Problem 7 -61) to yield propane is $-295 \mathrm{~kJ} / \mathrm{mol},$ and the heat of hydrogenation for a typical monosubstituted alkene, such as propene, is $-125 \mathrm{~kJ} / \mathrm{mol}$. Is allene more stable or less stable than you might expect for a diene? Explain.

Lainey Roebuck
Lainey Roebuck
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01:06

Problem 63

Retin A, or retinoic acid, is a medication commonly used to reduce wrinkles and treat severe acne. How many different isomers arising from double-bond isomerizations are possible?

Grigoriy Sereda
Grigoriy Sereda
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02:27

Problem 64

Fucoserratene and ectocarpene are sex pheromones produced by marine brown algae. What are their systematic names? (Ectocarpene is a bit difficult; make your best guess, and then check your answer in the Study Guide and Solutions Manual.)

Anand Jangid
Anand Jangid
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Problem 65

tert-Butyl esters $\left[\mathrm{RCO}_{2} \mathrm{C}\left(\mathrm{CH}_{3}\right)_{3}\right]$ are converted into carboxylic acids $\left(\mathrm{RCO}_{2} \mathrm{H}\right)$ by reaction with trifluoroacetic acid, a reaction useful in protein synthesis (Section 26-7). Assign $E, Z$ designation to the double bonds of both reactant and product in the following scheme, and explain why there is an apparent change in double-bond stereochemistry:

Lainey Roebuck
Lainey Roebuck
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01:55

Problem 66

Vinylcyclopropane reacts with HBr to yield a rearranged alkyl bromide. Follow the flow of electrons as represented by the curved arrows, show the structure of the carbocation intermediate in brackets, and show the structure of the final product.

Grigoriy Sereda
Grigoriy Sereda
Numerade Educator
01:46

Problem 67

Calculate the degree of unsaturation in each of the following formulas:
(a) Cholesterol, $\mathrm{C}_{27} \mathrm{H}_{46} \mathrm{O}$
(b) $\mathrm{DDT}, \mathrm{C}_{14} \mathrm{H}_{9} \mathrm{Cl}_{5}$
(c) Prostaglandin $\mathrm{E}_{1}, \mathrm{C}_{20} \mathrm{H}_{34} \mathrm{O}_{5}$
(d) Caffeine, $\mathrm{C}_{8} \mathrm{H}_{10} \mathrm{~N}_{4} \mathrm{O}_{2}$
(e) Cortisone, $\mathrm{C}_{21} \mathrm{H}_{28} \mathrm{O}_{5}$
(f) Atropine, $\mathrm{C}_{17} \mathrm{H}_{23} \mathrm{NO}_{3}$

Grigoriy Sereda
Grigoriy Sereda
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01:14

Problem 68

The isobutyl cation spontaneously rearranges to the tert-butyl cation by a hydride shift. Is the rearrangement exergonic or endergonic? Draw what you think the transition state for the hydride shift might look like according to the Hammond postulate.

Grigoriy Sereda
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Problem 69

Draw an energy diagram for the addition of $\mathrm{HBr}$ to 1 -pentene. Let one curve on your diagram show the formation of 1 -bromopentane product and another curve on the same diagram show the formation of 2-bromopentane product. Label the positions for all reactants, intermediates, and products. Which curve has the higher-energy carbocation intermediate? Which curve has the higher-energy first transition state?

Lainey Roebuck
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Problem 70

Sketch the transition-state structures involved in the reaction of HBr with 1-pentene (Problem 7-69). Tell whether each structure resembles reactant or product.

Lainey Roebuck
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Problem 71

Aromatic compounds such as benzene react with alkyl chlorides in the presence of $\mathrm{AlCl}_{3}$ catalyst to yield alkylbenzenes. This reaction occurs through a carbocation intermediate, formed by reaction of the alkyl chloride with $\mathrm{AlCl}_{3}\left(\mathrm{R}-\mathrm{Cl}+\mathrm{AlCl}_{3} \rightarrow \mathrm{R}^{+}+\mathrm{AlCl}_{4}^{-}\right) .$ How can you explain the observation that reaction of benzene with 1 -chloropropane yields isopropylbenzene as the major product?

Lainey Roebuck
Lainey Roebuck
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01:24

Problem 72

Reaction of 2,3 -dimethyl-1-butene with HBr leads to an alkyl bromide, $\mathrm{C}_{6} \mathrm{H}_{13} \mathrm{Br} .$ On treatment of this alkyl bromide with $\mathrm{KOH}$ in methanol, elimination of HBr occurs and a hydrocarbon that is isomeric with the starting alkene is formed. What is the structure of this hydrocarbon, and how do you think it is formed from the alkyl bromide?

Grigoriy Sereda
Grigoriy Sereda
Numerade Educator