(a) Interpretation: The conversion of acetophenone into the given compound is to be done. Concept introduction: When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Question

Want to see the full answer?

Answer 1

Question

Chapter 24, Problem 24.61P

Interpretation Introduction

(a)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Interpretation Introduction

(b)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Interpretation Introduction

(c)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Interpretation Introduction

(d)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

A pdf file of your hand drawn, stepwise mechanisms for the reactions. For each reaction in the assignment, you must write each mechanism three times (there are 10 reactions, so 30 mechanisms). (A) do the work on a tablet and save as a pdf., it is expected to write each mechanism out and NOT copy and paste the mechanism after writing it just once. Everything should be drawn out stepwise and every bond that is formed and broken in the process of the reaction, and is expected to see all relevant lone pair electrons and curved arrows.

None

Answer 2

Question

Chapter 24, Problem 24.61P

Interpretation Introduction

(a)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Interpretation Introduction

(b)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Interpretation Introduction

(c)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Interpretation Introduction

(d)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Chapter 24, Problem 24.61P

Interpretation Introduction

(a)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Interpretation Introduction

(b)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Interpretation Introduction

(c)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Interpretation Introduction

(d)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Chapter 24, Problem 24.61P

Interpretation Introduction

(a)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Interpretation Introduction

(b)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Interpretation Introduction

(c)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Interpretation Introduction

(d)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 24, Problem 24.61P

Interpretation Introduction

(a)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Interpretation Introduction

(b)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Interpretation Introduction

(c)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Interpretation Introduction

(d)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Answer 6

Chapter 24, Problem 24.61P

Interpretation Introduction

(a)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Answer 7

Chapter 24, Problem 24.61P

Interpretation Introduction

(a)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Answer 8

Interpretation Introduction

(b)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Answer 9

Interpretation Introduction

(b)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Answer 10

Interpretation Introduction

(c)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Answer 11

Interpretation Introduction

(c)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Answer 12

Interpretation Introduction

(d)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Answer 13

Interpretation Introduction

(d)

Interpretation:

The conversion of acetophenone into the given compound is to be done.

Concept introduction:

When only one carbonyl component has an alpha hydrogen atom, then a cross aldol reaction will occur. There will be formation of only one product. The yield of single cross aldol condensation reaction is enhanced if the electrophilic carbonyl compound is relatively unhindered.

Answer 14

Expert Solution & Answer

Answer 15

Expert Solution & Answer

Answer 16

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 17

Ch. 24 - Prob. 24.1P Ch. 24 - Prob. 24.2P Ch. 24 - Problem 24.3 What unsaturated carbonyl compound is...Ch. 24 - Acid-catalyzed dehydration of hydroxy carbonyl...Ch. 24 - Prob. 24.5P Ch. 24 - Prob. 24.6P Ch. 24 - Prob. 24.7P Ch. 24 - Problem 24.8 Draw the products formed in the...Ch. 24 - Prob. 24.9P Ch. 24 - Prob. 24.10P

Solution Summary: The author explains how acetophenone reacts with a base to form an enolate ion.

Concept explainers

Videos

Want to see the full answer?

Chapter 24 Solutions