(a) Interpretation: The structural formula of keto form for the given enol form should be drawn. Concept Introduction: A carbonyl compound that has a-hydrogen on a-carbon changes its form to enol through resonance. Both the form stays in equilibrium. a- hydrogen is the hydrogen which attached to a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergoes Keto-Enol tautomerism.

Question

A mixture of C7H12O2, C9H9OCl, biphenyl and acetone was put together in a gas chromatography tube. Please decide from the GC resutls which correspond to the peak for C7,C9 and biphenyl and explain the reasoning based on GC results. Eliminate unnecessary peaks from Gas Chromatography results.

Answer 1

Question

Chapter 17, Problem 17.45P

Interpretation Introduction

(a)

Interpretation:

The structural formula of keto form for the given enol form should be drawn.

Concept Introduction:

A carbonyl compound that has a-hydrogen on a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergoes Keto-Enol tautomerism.

Interpretation Introduction

(b)

Interpretation:

The structural formula of keto form for the given enol form should be drawn.

Concept Introduction:

A carbonyl compound that has a-hydrogen on a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergoes Keto-Enol tautomerism.

Interpretation Introduction

(c)

Interpretation:

The structural formula of keto form for the given enol form should be drawn.

Concept Introduction:

A carbonyl compound that has a-hydrogen on a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergoes Keto-Enol tautomerism.

Expert Solution & Answer

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Students have asked these similar questions

A mixture of C7H12O2, C9H9OCl, biphenyl and acetone was put together in a gas chromatography tube. Please decide from the GC resutls which correspond to the peak for C7,C9 and biphenyl and explain the reasoning based on GC results. Eliminate unnecessary peaks from Gas Chromatography results.

Is the molecule chiral, meso, or achiral? CI .CH3 H₂C CI

PLEASE HELP ! URGENT!

Answer 2

Question

Chapter 17, Problem 17.45P

Interpretation Introduction

(a)

Interpretation:

The structural formula of keto form for the given enol form should be drawn.

Concept Introduction:

A carbonyl compound that has a-hydrogen on a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergoes Keto-Enol tautomerism.

Interpretation Introduction

(b)

Interpretation:

The structural formula of keto form for the given enol form should be drawn.

Concept Introduction:

A carbonyl compound that has a-hydrogen on a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergoes Keto-Enol tautomerism.

Interpretation Introduction

(c)

Interpretation:

The structural formula of keto form for the given enol form should be drawn.

Concept Introduction:

A carbonyl compound that has a-hydrogen on a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergoes Keto-Enol tautomerism.

Expert Solution & Answer

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Answer 3

Question

Chapter 17, Problem 17.45P

Interpretation Introduction

(a)

Interpretation:

The structural formula of keto form for the given enol form should be drawn.

Concept Introduction:

A carbonyl compound that has a-hydrogen on a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergoes Keto-Enol tautomerism.

Interpretation Introduction

(b)

Interpretation:

The structural formula of keto form for the given enol form should be drawn.

Concept Introduction:

A carbonyl compound that has a-hydrogen on a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergoes Keto-Enol tautomerism.

Interpretation Introduction

(c)

Interpretation:

The structural formula of keto form for the given enol form should be drawn.

Concept Introduction:

A carbonyl compound that has a-hydrogen on a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergoes Keto-Enol tautomerism.

Expert Solution & Answer

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Answer 4

Question

Chapter 17, Problem 17.45P

Interpretation Introduction

(a)

Interpretation:

The structural formula of keto form for the given enol form should be drawn.

Concept Introduction:

A carbonyl compound that has a-hydrogen on a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergoes Keto-Enol tautomerism.

Interpretation Introduction

(b)

Interpretation:

The structural formula of keto form for the given enol form should be drawn.

Concept Introduction:

A carbonyl compound that has a-hydrogen on a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergoes Keto-Enol tautomerism.

Interpretation Introduction

(c)

Interpretation:

The structural formula of keto form for the given enol form should be drawn.

Concept Introduction:

A carbonyl compound that has a-hydrogen on a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergoes Keto-Enol tautomerism.

Expert Solution & Answer

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Answer 5

Chapter 17, Problem 17.45P

Interpretation Introduction

(a)

Interpretation:

The structural formula of keto form for the given enol form should be drawn.

Concept Introduction:

A carbonyl compound that has a-hydrogen on a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergoes Keto-Enol tautomerism.

Interpretation Introduction

(b)

Interpretation:

The structural formula of keto form for the given enol form should be drawn.

Concept Introduction:

A carbonyl compound that has a-hydrogen on a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergoes Keto-Enol tautomerism.

Interpretation Introduction

(c)

Interpretation:

The structural formula of keto form for the given enol form should be drawn.

Concept Introduction:

A carbonyl compound that has a-hydrogen on a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergoes Keto-Enol tautomerism.

Answer 6

Chapter 17, Problem 17.45P

Interpretation Introduction

(a)

Interpretation:

The structural formula of keto form for the given enol form should be drawn.

Concept Introduction:

A carbonyl compound that has a-hydrogen on a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergoes Keto-Enol tautomerism.

Answer 7

Chapter 17, Problem 17.45P

Interpretation Introduction

(a)

Interpretation:

The structural formula of keto form for the given enol form should be drawn.

Concept Introduction:

A carbonyl compound that has a-hydrogen on a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergoes Keto-Enol tautomerism.

Answer 8

Interpretation Introduction

(b)

Interpretation:

The structural formula of keto form for the given enol form should be drawn.

Concept Introduction:

A carbonyl compound that has a-hydrogen on a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergoes Keto-Enol tautomerism.

Answer 9

Interpretation Introduction

(b)

Interpretation:

The structural formula of keto form for the given enol form should be drawn.

Concept Introduction:

A carbonyl compound that has a-hydrogen on a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergoes Keto-Enol tautomerism.

Answer 10

Interpretation Introduction

(c)

Interpretation:

The structural formula of keto form for the given enol form should be drawn.

Concept Introduction:

A carbonyl compound that has a-hydrogen on a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergoes Keto-Enol tautomerism.

Answer 11

Interpretation Introduction

(c)

Interpretation:

The structural formula of keto form for the given enol form should be drawn.

Concept Introduction:

A carbonyl compound that has a-hydrogen on a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergoes Keto-Enol tautomerism.

Answer 12

Expert Solution & Answer

Answer 13

Expert Solution & Answer

Answer 14

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Answer 15

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Answer 16

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Answer 17

Trending nowThis is a popular solution!

Answer 18

Trending nowThis is a popular solution!

Answer 19

Trending nowThis is a popular solution!

Answer 20

Trending now

Answer 21

This is a popular solution!

Answer 22

See solution

Check out sample textbook solution

Answer 23

Ch. 17.2 - Problem 17-1 Wrtie the IUPAC name for each...Ch. 17.2 - Prob. 17.2P Ch. 17.2 - Prob. 17.3P Ch. 17.4 - Prob. 17.4P Ch. 17.4 - Prob. 17.5P Ch. 17.4 - Problem 17-6 Show the reaction of benzaldehyde...Ch. 17.4 - Problem 17-7 Identify all hemiacetals and acetals...Ch. 17.5 - Prob. 17.8P Ch. 17 - 17-9 Answer true or false. (a) The one aldehyde...Ch. 17 - Prob. 17.10P

Solution Summary: The author explains the structural formula of keto form for the given enol form.

Concept explainers

Chapter 17 Solutions