Fatty-acid biosynthesis (Figure 29-5), acetoacetyl ACP is reduced stereospecifically by NADPH to yield an alcohol and explain hydride ion add to the Si face or the Re face of acetoacetyl ACP.

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Answer 1

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Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 29.SE, Problem 54AP

Interpretation Introduction

Interpretation:

Fatty-acid biosynthesis (Figure 29-5), acetoacetyl ACP is reduced stereospecifically by NADPH to yield an alcohol and explain hydride ion add to the Si face or the Re face of acetoacetyl ACP.

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Answer 2

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Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 29.SE, Problem 54AP

Interpretation Introduction

Interpretation:

Fatty-acid biosynthesis (Figure 29-5), acetoacetyl ACP is reduced stereospecifically by NADPH to yield an alcohol and explain hydride ion add to the Si face or the Re face of acetoacetyl ACP.

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Answer 3

Question

Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 29.SE, Problem 54AP

Interpretation Introduction

Interpretation:

Fatty-acid biosynthesis (Figure 29-5), acetoacetyl ACP is reduced stereospecifically by NADPH to yield an alcohol and explain hydride ion add to the Si face or the Re face of acetoacetyl ACP.

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Answer 4

Question

Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 29.SE, Problem 54AP

Interpretation Introduction

Interpretation:

Fatty-acid biosynthesis (Figure 29-5), acetoacetyl ACP is reduced stereospecifically by NADPH to yield an alcohol and explain hydride ion add to the Si face or the Re face of acetoacetyl ACP.

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Answer 5

Chapter 29.SE, Problem 54AP

Interpretation Introduction

Interpretation:

Fatty-acid biosynthesis (Figure 29-5), acetoacetyl ACP is reduced stereospecifically by NADPH to yield an alcohol and explain hydride ion add to the Si face or the Re face of acetoacetyl ACP.

Answer 6

Chapter 29.SE, Problem 54AP

Interpretation Introduction

Interpretation:

Fatty-acid biosynthesis (Figure 29-5), acetoacetyl ACP is reduced stereospecifically by NADPH to yield an alcohol and explain hydride ion add to the Si face or the Re face of acetoacetyl ACP.

Answer 7

Chapter 29.SE, Problem 54AP

Interpretation Introduction

Interpretation:

Fatty-acid biosynthesis (Figure 29-5), acetoacetyl ACP is reduced stereospecifically by NADPH to yield an alcohol and explain hydride ion add to the Si face or the Re face of acetoacetyl ACP.

Answer 8

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Answer 9

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Answer 10

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Answer 11

Ch. 29.1 - Prob. 1P Ch. 29.3 - Write the equations for the remaining passages of...Ch. 29.3 - Prob. 3P Ch. 29.4 - Write a mechanism for the dehydration reaction of...Ch. 29.4 - Evidence for the role of acetate in fatty-acid...Ch. 29.4 - Does the reduction of acetoacetyl ACP in step 6...Ch. 29.5 - Prob. 7P Ch. 29.5 - Look at the entire glycolysis pathway, and make a...Ch. 29.6 - Prob. 9P Ch. 29.7 - Prob. 10P

Fatty-acid biosynthesis (Figure 29-5), acetoacetyl ACP is reduced stereospecifically by NADPH to yield an alcohol and explain hydride ion add to the Si face or the Re face of acetoacetyl ACP.

Solution Summary: The author explains that hydride ion adds to the Si face or the Re face of acetoacetyl ACP, a prochiral concept of addition.

Concept explainers

Interpretation:

Fatty-acid biosynthesis (Figure 29-5), acetoacetyl ACP is reduced stereospecifically by NADPH to yield an alcohol and explain hydride ion add to the Si face or the Re face of acetoacetyl ACP.

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Chapter 29 Solutions

Fatty-acid biosynthesis (Figure 29-5), acetoacetyl ACP is reduced stereospecifically by NADPH to yield an alcohol and explain hydride ion add to the Si face or the Re face of acetoacetyl ACP.

Solution Summary: The author explains that hydride ion adds to the Si face or the Re face of acetoacetyl ACP, a prochiral concept of addition.

Concept explainers

Interpretation: Fatty-acid biosynthesis (Figure 29-5), acetoacetyl ACP is reduced stereospecifically by NADPH to yield an alcohol and explain hydride ion add to the Si face or the Re face of acetoacetyl ACP.

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Chapter 29 Solutions

Interpretation:

Fatty-acid biosynthesis (Figure 29-5), acetoacetyl ACP is reduced stereospecifically by NADPH to yield an alcohol and explain hydride ion add to the Si face or the Re face of acetoacetyl ACP.