(a) Interpretation: The structure for 2-phenyl-1-hexene is to be drawn. Concept introduction: Benzene derivatives are named by considering the root as benzene. If the substituents attached to a benzene ring are complicated, it is easy to treat the benzene ring as a substituent instead of a root. These substituents are incorporated into the IUPAC name.

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Answer 1

Question

Chapter B, Problem B.14P

Interpretation Introduction

(a)

Interpretation:

The structure for 2-phenyl-1-hexene is to be drawn.

Concept introduction:

Benzene derivatives are named by considering the root as benzene. If the substituents attached to a benzene ring are complicated, it is easy to treat the benzene ring as a substituent instead of a root. These substituents are incorporated into the IUPAC name.

Interpretation Introduction

(b)

Interpretation:

The structure for 1, 5-diphenylpentane is to be drawn.

Concept introduction:

Benzene derivatives are named by considering the root as benzene. If the substituents attached to a benzene ring are complicated, it is easy to treat the benzene ring as a substituent instead of a root. These substituents are incorporated into the IUPAC name.

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Please help with number 6 I got a negative number could that be right?

1,4-Dimethyl-1,3-cyclohexadiene can undergo 1,2- or 1,4-addition with hydrogen halides. (a) 1,2-Addition i. Draw the carbocation intermediate(s) formed during the 1,2-addition of hydrobromic acid to 1,4-dimethyl-1,3-cyclohexadiene. ii. What is the major 1,2-addition product formed during the reaction in (i)? (b) 1,4-Addition i. Draw the carbocation intermediate(s) formed during the 1,4-addition of hydrobromic acid to 1,4-dimethyl-1,3-cyclohexadiene. ii. What is the major 1,4-addition product formed from the reaction in (i)? (c) What is the kinetic product from the reaction of one mole of hydrobromic acid with 1,4-dimethyl-1,3-cyclohexadiene? Explain your reasoning. (d) What is the thermodynamic product from the reaction of one mole of hydrobro-mic acid with 1,4-dimethyl-1,3-cyclohexadiene? Explain your reasoning. (e) What major product will result when 1,4-dimethyl-1,3-cyclohexadiene is treated with one mole of hydrobromic acid at - 78 deg * C ? Explain your reasoning.

Give the product of the bimolecular elimination from each of the isomeric halogenated compounds. Reaction A Reaction B. КОВ CH₂ HotBu +B+ ко HOIBU +Br+ Templates More QQQ Select Cv Templates More Cras QQQ One of these compounds undergoes elimination 50x faster than the other. Which one and why? Reaction A because the conformation needed for elimination places the phenyl groups and to each other Reaction A because the conformation needed for elimination places the phenyl groups gauche to each other. ◇ Reaction B because the conformation needed for elimination places the phenyl groups gach to each other. Reaction B because the conformation needed for elimination places the phenyl groups anti to each other.

Answer 2

Question

Chapter B, Problem B.14P

Interpretation Introduction

(a)

Interpretation:

The structure for 2-phenyl-1-hexene is to be drawn.

Concept introduction:

Benzene derivatives are named by considering the root as benzene. If the substituents attached to a benzene ring are complicated, it is easy to treat the benzene ring as a substituent instead of a root. These substituents are incorporated into the IUPAC name.

Interpretation Introduction

(b)

Interpretation:

The structure for 1, 5-diphenylpentane is to be drawn.

Concept introduction:

Benzene derivatives are named by considering the root as benzene. If the substituents attached to a benzene ring are complicated, it is easy to treat the benzene ring as a substituent instead of a root. These substituents are incorporated into the IUPAC name.

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Answer 3

Question

Chapter B, Problem B.14P

Interpretation Introduction

(a)

Interpretation:

The structure for 2-phenyl-1-hexene is to be drawn.

Concept introduction:

Benzene derivatives are named by considering the root as benzene. If the substituents attached to a benzene ring are complicated, it is easy to treat the benzene ring as a substituent instead of a root. These substituents are incorporated into the IUPAC name.

Interpretation Introduction

(b)

Interpretation:

The structure for 1, 5-diphenylpentane is to be drawn.

Concept introduction:

Benzene derivatives are named by considering the root as benzene. If the substituents attached to a benzene ring are complicated, it is easy to treat the benzene ring as a substituent instead of a root. These substituents are incorporated into the IUPAC name.

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Answer 4

Question

Chapter B, Problem B.14P

Interpretation Introduction

(a)

Interpretation:

The structure for 2-phenyl-1-hexene is to be drawn.

Concept introduction:

Benzene derivatives are named by considering the root as benzene. If the substituents attached to a benzene ring are complicated, it is easy to treat the benzene ring as a substituent instead of a root. These substituents are incorporated into the IUPAC name.

Interpretation Introduction

(b)

Interpretation:

The structure for 1, 5-diphenylpentane is to be drawn.

Concept introduction:

Benzene derivatives are named by considering the root as benzene. If the substituents attached to a benzene ring are complicated, it is easy to treat the benzene ring as a substituent instead of a root. These substituents are incorporated into the IUPAC name.

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Answer 5

Chapter B, Problem B.14P

Interpretation Introduction

(a)

Interpretation:

The structure for 2-phenyl-1-hexene is to be drawn.

Concept introduction:

Benzene derivatives are named by considering the root as benzene. If the substituents attached to a benzene ring are complicated, it is easy to treat the benzene ring as a substituent instead of a root. These substituents are incorporated into the IUPAC name.

Interpretation Introduction

(b)

Interpretation:

The structure for 1, 5-diphenylpentane is to be drawn.

Concept introduction:

Benzene derivatives are named by considering the root as benzene. If the substituents attached to a benzene ring are complicated, it is easy to treat the benzene ring as a substituent instead of a root. These substituents are incorporated into the IUPAC name.

Answer 6

Chapter B, Problem B.14P

Interpretation Introduction

(a)

Interpretation:

The structure for 2-phenyl-1-hexene is to be drawn.

Concept introduction:

Benzene derivatives are named by considering the root as benzene. If the substituents attached to a benzene ring are complicated, it is easy to treat the benzene ring as a substituent instead of a root. These substituents are incorporated into the IUPAC name.

Answer 7

Chapter B, Problem B.14P

Interpretation Introduction

(a)

Interpretation:

The structure for 2-phenyl-1-hexene is to be drawn.

Concept introduction:

Benzene derivatives are named by considering the root as benzene. If the substituents attached to a benzene ring are complicated, it is easy to treat the benzene ring as a substituent instead of a root. These substituents are incorporated into the IUPAC name.

Answer 8

Interpretation Introduction

(b)

Interpretation:

The structure for 1, 5-diphenylpentane is to be drawn.

Concept introduction:

Benzene derivatives are named by considering the root as benzene. If the substituents attached to a benzene ring are complicated, it is easy to treat the benzene ring as a substituent instead of a root. These substituents are incorporated into the IUPAC name.

Answer 9

Interpretation Introduction

(b)

Interpretation:

The structure for 1, 5-diphenylpentane is to be drawn.

Concept introduction:

Benzene derivatives are named by considering the root as benzene. If the substituents attached to a benzene ring are complicated, it is easy to treat the benzene ring as a substituent instead of a root. These substituents are incorporated into the IUPAC name.

Answer 10

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Answer 11

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Answer 12

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Answer 13

Ch. B - Prob. B.1P Ch. B - Prob. B.2P Ch. B - Prob. B.3P Ch. B - Prob. B.4P Ch. B - Prob. B.5P Ch. B - Prob. B.6P Ch. B - Prob. B.7P Ch. B - Prob. B.8P Ch. B - Prob. B.9P Ch. B - Prob. B.10P

Solution Summary: The author explains the structure of the compound 2-phenyl-1-hexene.

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