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.

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 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.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Products obtained from this structure

The biochemical degradation of isoleucine goes through the intermediate tiglyl‑CoA, shown as the starting material in the scheme. This route is similar to the β‑oxidation of fatty acids. Complete the structure of the intermediate and product of this reaction. The carbon skeleton and acetyl CoA thioester have been predrawn for you. Do not delete any atoms or bonds.

Water production from fatty acid oxidation is a survival mechanism in animals where water is scarce. Cells oxidize palmitoyl-CoA to produce water. If an animal has 5.000 kg of palmitoyl-CoA available for fatty acid oxidation, how many kilograms of water could the animal produce from that palmitoyl-CoA? The chemical formula for palmitoyl-CoA is C37H66N7O17P3S.

Answer 2

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.

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 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.

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 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.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

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

Expert Solution & Answer

Answer 9

Expert Solution & Answer

Answer 10

Want to see the full answer?

Check out a sample textbook solution

See solution

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.

Want to see the full answer?

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.

Want to see the full answer?

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.