Get Ready for Organic Chemistry
Get Ready for Organic Chemistry
2nd Edition
ISBN: 9780321774125
Author: KARTY, Joel
Publisher: PEARSON
bartleby

Concept explainers

bartleby

Videos

Question
Book Icon
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.

Blurred answer
Students have asked these similar questions
2. Provide a clear arrow-pushing mechanism for the following reactions. Do not skip proton transfers, do not combine steps, and make sure your arrows are clear enough to be interpreted without ambiguity. a. CH3 Ph OEt هد Ph CH3 Hint: the species on the left is an ynolate, which behaves a lot like an enolate.
b. CH3 H3C CH3 CH3 H3C an unexpected product, containing a single 9- membered ring the expected product, containing two fused rings H3C-I (H3C)2CuLi an enolate
b. H3C CH3 1. 2. H3O+ H3C MgBr H3C

Chapter 7 Solutions

Get Ready for Organic Chemistry

Knowledge Booster
Background pattern image
Chemistry
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning
Coenzymes and cofactors; Author: CH15 SWAYAM Prabha IIT Madras;https://www.youtube.com/watch?v=bubY2Nm7hVM;License: Standard YouTube License, CC-BY
Aromaticity and Huckel's Rule; Author: Professor Dave Explains;https://www.youtube.com/watch?v=7-BguH4_WBQ;License: Standard Youtube License