Organic Chemistry: A Guided Inquiry
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN: 9780618974122
Author: Andrei Straumanis
Publisher: Cengage Learning
bartleby

Concept explainers

Question
Book Icon
Chapter 8, Problem 31CTQ

a)

Interpretation Introduction

Interpretation: Whether H2O act as nucleophile or electrophile in step 2 of below reaction should be determined.

  Organic Chemistry: A Guided Inquiry, Chapter 8, Problem 31CTQ , additional homework tip  1

Concept introduction: The carbon-carbon double bond in alkene consists of a strong σ bond (formed by overlap of sp2 hybridized orbital on each carbon) and a weak π bond (formed by overlap of pure p orbital on each carbon). Due to unsaturation, alkene shows addition reaction where the double bond provides loosely held π electrons and is readily attacked by any electron deficient group like H+ ions released from acids. The loosely held π electrons are present, therefore, behave as base though weak one.

b)

Interpretation Introduction

Interpretation: Whether H of H3O+ act as nucleophile or electrophile in step 1 of below reaction should be determined.

  Organic Chemistry: A Guided Inquiry, Chapter 8, Problem 31CTQ , additional homework tip  2

Concept introduction: The carbon-carbon double bond in alkene consists of a strong σ bond (formed by overlap of sp2 hybridized orbital on each carbon) and a weak π bond (formed by overlap of pure p orbital on each carbon). Due to unsaturation, alkene shows addition reaction where the double bond provides loosely held π electrons and is readily attacked by any electron deficient group like H+ ions released from acids. The loosely held π electrons are present, therefore, behave as base though weak one.

Blurred answer
Students have asked these similar questions
6. Place an "X" in the box below the nucleophile that will react the most quickly with methyl iodide. Place an "O" in the box below the nucleophile that will react the most slowly with methyl iodide.
Consider this nucleophilic substitution reaction.   1. Highlight the electrophilic carbon in red, and highlight the leaving group in blue. Highlight the atom in the nucleophile that will attack the electrophilic center in green. Only atoms need to be highlighted and not the lone pairs or formal charges. 2. Draw the product(s) of the reaction. Include all lone pairs.
This is a umplong reaction. I'm looking for what reagent and intermediates would look like. Thank you

Chapter 8 Solutions

Organic Chemistry: A Guided Inquiry

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
Recommended textbooks for you
Text book image
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning