(a) Interpretation: The carbonyl compound needed to produce the following alcohol by a reduction reaction should be determined: CH 3 CH 2 CH 2 CH 2 CH 2 OH Concept Introduction: In a reduction of an organic molecule, either the number of C-O bonds decreases or number of C-H bonds increases. So when an aldehyde is reduced by H 2 in the presence of Pd catalyst, C=O double bond is reduced to C-O single bond and H 2 is added across this C=O double bond forming a primary alcohol.

Question

Want to see the full answer?

Answer 1

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 16, Problem 16.63P

Interpretation Introduction

(a)

Interpretation:

The carbonyl compound needed to produce the following alcohol by a reduction reaction should be determined:

CH₃CH₂CH₂CH₂CH₂OH

Concept Introduction:

In a reduction of an organic molecule, either the number of C-O bonds decreases or number of C-H bonds increases. So when an aldehyde is reduced by H₂ in the presence of Pd catalyst, C=O double bond is reduced to C-O single bond and H₂ is added across this C=O double bond forming a primary alcohol.

Interpretation Introduction

(b)

Interpretation:

The carbonyl compound needed to produce the following alcohol by a reduction reaction should be determined:

Concept Introduction:

In a reduction of an organic molecule, either the number of C-O bonds decreases or number of C-H bonds increases. So when a ketone is reduced by H₂ in the presence of Pd catalyst, C=O double bond is reduced to C-O single bond and H₂ is added across this C=O double bond forming a secondary alcohol.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Predict the major products of this organic reaction: HBr (1 equiv) cold ? Some important notes: • Draw the major product, or products, of this reaction in the drawing area below. • You can draw the products in any arrangement you like. • Pay careful attention to the reaction conditions, and only include the major products. • Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers. • Note that there is only 1 equivalent of HBr reactant, so you need not consider the case of multiple additions. Erase something Explanation Check 2025 McGraw Hill LLC. All Rights Reserved. Ter

Q14. Fill this chart: (please refer to ppt notes/browser to answer these questions) What alcohol is also called wood alcohol? What is the common name of ethanol? Draw the structure of phenol and thiophene? Are bigger chain alcohol like heptanol and octanol are soluble or insoluble in water and explain it ? Are ethers soluble or insoluble in water? What suffix and prefix are used for alcohol while naming alcohol and ether? What the process called when we add water to any alkene to make alcohol? Q16. Draw the diagram of following aromatic compound (practice from previous module) Aniline Phenol Benzoic acid Methyl benzoate Q17. a. Write the oxidation reactions for the 2 propanol. b. Write the oxidation reaction of the ethanol.

Question 11 of 18 (1 point) Question Attempt: 3 of How many signals do you expect in the 'H NMR spectrum for this molecule? Br Br Write the answer below. Also, in each of the drawing areas below is a copy of the molecule, with Hs shown. In each copy, one of the H atoms is colored red. Highlight in red all other H atoms that would contribute to the same signal as the H already highlighted red. Note for advanced students: In this question, any multiplet is counted as one signal. Number of signals in the 'H NMR spectrum. 1 For the molecule in the top drawing area, highlight in red any other H atoms that will contribute to the same signal as the H atom already highlighted red. If no other H atoms will contribute, check the box at right. No additional Hs to color in top molecule Check For the molecule in the bottom drawing area, highlight in red any other H atoms that will contribute to the same signal as the H atom already highlighted red. If no other H atoms will contribute, check the box…

Answer 2

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 16, Problem 16.63P

Interpretation Introduction

(a)

Interpretation:

The carbonyl compound needed to produce the following alcohol by a reduction reaction should be determined:

CH₃CH₂CH₂CH₂CH₂OH

Concept Introduction:

In a reduction of an organic molecule, either the number of C-O bonds decreases or number of C-H bonds increases. So when an aldehyde is reduced by H₂ in the presence of Pd catalyst, C=O double bond is reduced to C-O single bond and H₂ is added across this C=O double bond forming a primary alcohol.

Interpretation Introduction

(b)

Interpretation:

The carbonyl compound needed to produce the following alcohol by a reduction reaction should be determined:

Concept Introduction:

In a reduction of an organic molecule, either the number of C-O bonds decreases or number of C-H bonds increases. So when a ketone is reduced by H₂ in the presence of Pd catalyst, C=O double bond is reduced to C-O single bond and H₂ is added across this C=O double bond forming a secondary alcohol.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 16, Problem 16.63P

Interpretation Introduction

(a)

Interpretation:

The carbonyl compound needed to produce the following alcohol by a reduction reaction should be determined:

CH₃CH₂CH₂CH₂CH₂OH

Concept Introduction:

In a reduction of an organic molecule, either the number of C-O bonds decreases or number of C-H bonds increases. So when an aldehyde is reduced by H₂ in the presence of Pd catalyst, C=O double bond is reduced to C-O single bond and H₂ is added across this C=O double bond forming a primary alcohol.

Interpretation Introduction

(b)

Interpretation:

The carbonyl compound needed to produce the following alcohol by a reduction reaction should be determined:

Concept Introduction:

In a reduction of an organic molecule, either the number of C-O bonds decreases or number of C-H bonds increases. So when a ketone is reduced by H₂ in the presence of Pd catalyst, C=O double bond is reduced to C-O single bond and H₂ is added across this C=O double bond forming a secondary alcohol.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 16, Problem 16.63P

Interpretation Introduction

(a)

Interpretation:

The carbonyl compound needed to produce the following alcohol by a reduction reaction should be determined:

CH₃CH₂CH₂CH₂CH₂OH

Concept Introduction:

In a reduction of an organic molecule, either the number of C-O bonds decreases or number of C-H bonds increases. So when an aldehyde is reduced by H₂ in the presence of Pd catalyst, C=O double bond is reduced to C-O single bond and H₂ is added across this C=O double bond forming a primary alcohol.

Interpretation Introduction

(b)

Interpretation:

The carbonyl compound needed to produce the following alcohol by a reduction reaction should be determined:

Concept Introduction:

In a reduction of an organic molecule, either the number of C-O bonds decreases or number of C-H bonds increases. So when a ketone is reduced by H₂ in the presence of Pd catalyst, C=O double bond is reduced to C-O single bond and H₂ is added across this C=O double bond forming a secondary alcohol.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 16, Problem 16.63P

Interpretation Introduction

(a)

Interpretation:

The carbonyl compound needed to produce the following alcohol by a reduction reaction should be determined:

CH₃CH₂CH₂CH₂CH₂OH

Concept Introduction:

In a reduction of an organic molecule, either the number of C-O bonds decreases or number of C-H bonds increases. So when an aldehyde is reduced by H₂ in the presence of Pd catalyst, C=O double bond is reduced to C-O single bond and H₂ is added across this C=O double bond forming a primary alcohol.

Interpretation Introduction

(b)

Interpretation:

The carbonyl compound needed to produce the following alcohol by a reduction reaction should be determined:

Concept Introduction:

In a reduction of an organic molecule, either the number of C-O bonds decreases or number of C-H bonds increases. So when a ketone is reduced by H₂ in the presence of Pd catalyst, C=O double bond is reduced to C-O single bond and H₂ is added across this C=O double bond forming a secondary alcohol.

Answer 6

Chapter 16, Problem 16.63P

Interpretation Introduction

(a)

Interpretation:

The carbonyl compound needed to produce the following alcohol by a reduction reaction should be determined:

CH₃CH₂CH₂CH₂CH₂OH

Concept Introduction:

In a reduction of an organic molecule, either the number of C-O bonds decreases or number of C-H bonds increases. So when an aldehyde is reduced by H₂ in the presence of Pd catalyst, C=O double bond is reduced to C-O single bond and H₂ is added across this C=O double bond forming a primary alcohol.

Answer 7

Chapter 16, Problem 16.63P

Interpretation Introduction

(a)

Interpretation:

The carbonyl compound needed to produce the following alcohol by a reduction reaction should be determined:

CH₃CH₂CH₂CH₂CH₂OH

Concept Introduction:

In a reduction of an organic molecule, either the number of C-O bonds decreases or number of C-H bonds increases. So when an aldehyde is reduced by H₂ in the presence of Pd catalyst, C=O double bond is reduced to C-O single bond and H₂ is added across this C=O double bond forming a primary alcohol.

Answer 8

Interpretation Introduction

(b)

Interpretation:

The carbonyl compound needed to produce the following alcohol by a reduction reaction should be determined:

Concept Introduction:

In a reduction of an organic molecule, either the number of C-O bonds decreases or number of C-H bonds increases. So when a ketone is reduced by H₂ in the presence of Pd catalyst, C=O double bond is reduced to C-O single bond and H₂ is added across this C=O double bond forming a secondary alcohol.

Answer 9

Interpretation Introduction

(b)

Interpretation:

The carbonyl compound needed to produce the following alcohol by a reduction reaction should be determined:

Concept Introduction:

In a reduction of an organic molecule, either the number of C-O bonds decreases or number of C-H bonds increases. So when a ketone is reduced by H₂ in the presence of Pd catalyst, C=O double bond is reduced to C-O single bond and H₂ is added across this C=O double bond forming a secondary alcohol.

Answer 10

Expert Solution & Answer

Answer 11

Expert Solution & Answer

Answer 12

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 13

Ch. 16.1 - Prob. 16.1P Ch. 16.1 - Draw the structure of the three constitutional...Ch. 16.2 - Prob. 16.3P Ch. 16.2 - Give the structure corresponding to each TUPAC...Ch. 16.2 - Prob. 16.5P Ch. 16.2 - Prob. 16.6P Ch. 16.2 - Give the structure corresponding to each name. a....Ch. 16.3 - Which compound in each pair has the higher boiling...Ch. 16.3 - Acetone and progesterone are two ketones that...Ch. 16.4 - Prob. 16.10P

Solution Summary: The author explains the carbonyl compound needed to produce the following alcohol by a reduction reaction.

Concept explainers

Want to see the full answer?

Chapter 16 Solutions