(a) Interpretation: The product for the given nucleophilic addition step with appropriate curved arrows is to be drawn. Concept introduction: In the nucleophilic addition step, the nucleophile adds to the polar π bond. The nucleophile is relatively electron rich, and the polar π bond is relatively electron poor. Thus, the curved arrow drawn from the nucleophile to the polar π bond represents the flow of electrons from an electron rich site to an electron poor site. The first curved arrow is drawn from the negatively charged atom of the nucleophile to the less electronegative atom of the polar π bond, and the second curved arrow is drawn from the less electronegative atom to the double bonded more electronegative atom. The atom bonded to metal acts as a nucleophile.

Question

Draw the product of the reaction shown below. Ignore inorganic byproducts. H conc. HBr Drawing Q

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 7, Problem 7.13P

Interpretation Introduction

(a)

Interpretation:

The product for the given nucleophilic addition step with appropriate curved arrows is to be drawn.

Concept introduction:

In the nucleophilic addition step, the nucleophile adds to the polar π bond. The nucleophile is relatively electron rich, and the polar π bond is relatively electron poor. Thus, the curved arrow drawn from the nucleophile to the polar π bond represents the flow of electrons from an electron rich site to an electron poor site. The first curved arrow is drawn from the negatively charged atom of the nucleophile to the less electronegative atom of the polar π bond, and the second curved arrow is drawn from the less electronegative atom to the double bonded more electronegative atom. The atom bonded to metal acts as a nucleophile.

Interpretation Introduction

(b)

Interpretation:

The product for the given nucleophilic addition step with appropriate curved arrows is to be drawn.

Concept introduction:

In the nucleophilic addition step, the nucleophile adds to the polar π bond. The nucleophile is relatively electron rich, and the polar π bond is relatively electron poor. Thus, the curved arrow drawn from the nucleophile to the polar π bond represents the flow of electrons from an electron rich site to an electron poor site. The first curved arrow is drawn from the negatively charged atom of the nucleophile to the less electronegative atom of the polar π bond, and the second curved arrow is drawn from the less electronegative atom to the double bonded more electronegative atom. The atom bonded to metal acts as a nucleophile.

Expert Solution & Answer

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Students have asked these similar questions

Draw the product of the reaction shown below. Ignore inorganic byproducts. H conc. HBr Drawing Q

Calculate the atomic packing factor of diamond knowing that the number of Si atoms per cm3 is 2.66·1022 and that the atomic radii of silicon and oxygen are, respectively, 0.038 and 0.117 nm.

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. Aldol: NaOH HO H Δ NaOH Δ

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 7, Problem 7.13P

Interpretation Introduction

(a)

Interpretation:

The product for the given nucleophilic addition step with appropriate curved arrows is to be drawn.

Concept introduction:

In the nucleophilic addition step, the nucleophile adds to the polar π bond. The nucleophile is relatively electron rich, and the polar π bond is relatively electron poor. Thus, the curved arrow drawn from the nucleophile to the polar π bond represents the flow of electrons from an electron rich site to an electron poor site. The first curved arrow is drawn from the negatively charged atom of the nucleophile to the less electronegative atom of the polar π bond, and the second curved arrow is drawn from the less electronegative atom to the double bonded more electronegative atom. The atom bonded to metal acts as a nucleophile.

Interpretation Introduction

(b)

Interpretation:

The product for the given nucleophilic addition step with appropriate curved arrows is to be drawn.

Concept introduction:

In the nucleophilic addition step, the nucleophile adds to the polar π bond. The nucleophile is relatively electron rich, and the polar π bond is relatively electron poor. Thus, the curved arrow drawn from the nucleophile to the polar π bond represents the flow of electrons from an electron rich site to an electron poor site. The first curved arrow is drawn from the negatively charged atom of the nucleophile to the less electronegative atom of the polar π bond, and the second curved arrow is drawn from the less electronegative atom to the double bonded more electronegative atom. The atom bonded to metal acts as a nucleophile.

Expert Solution & Answer

Trending nowThis is a popular solution!

See solution

Check out sample textbook 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 7, Problem 7.13P

Interpretation Introduction

(a)

Interpretation:

The product for the given nucleophilic addition step with appropriate curved arrows is to be drawn.

Concept introduction:

In the nucleophilic addition step, the nucleophile adds to the polar π bond. The nucleophile is relatively electron rich, and the polar π bond is relatively electron poor. Thus, the curved arrow drawn from the nucleophile to the polar π bond represents the flow of electrons from an electron rich site to an electron poor site. The first curved arrow is drawn from the negatively charged atom of the nucleophile to the less electronegative atom of the polar π bond, and the second curved arrow is drawn from the less electronegative atom to the double bonded more electronegative atom. The atom bonded to metal acts as a nucleophile.

Interpretation Introduction

(b)

Interpretation:

The product for the given nucleophilic addition step with appropriate curved arrows is to be drawn.

Concept introduction:

In the nucleophilic addition step, the nucleophile adds to the polar π bond. The nucleophile is relatively electron rich, and the polar π bond is relatively electron poor. Thus, the curved arrow drawn from the nucleophile to the polar π bond represents the flow of electrons from an electron rich site to an electron poor site. The first curved arrow is drawn from the negatively charged atom of the nucleophile to the less electronegative atom of the polar π bond, and the second curved arrow is drawn from the less electronegative atom to the double bonded more electronegative atom. The atom bonded to metal acts as a nucleophile.

Expert Solution & Answer

Trending nowThis is a popular solution!

See solution

Check out sample textbook 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 7, Problem 7.13P

Interpretation Introduction