Step 1: Formation of the nucleophile - tert- butoxide ion NaO-t-Bu + H2O → Na+ + OH- + O-t-Bu Step 2: Nucleophilic attack by the tert- butoxide ion on the isopropyl chloride O-t-Bu- + (CH3)2CHCI → (CH3)2CHO-t-Bu + CI-

icon
Related questions
Question
Draw the molecular structure. Correctly solution please
Step 1: Formation of the nucleophile -tert-
butoxide ion
NaO-t-Bu + H2O → Na+ + OH- + O-t-Bu
Step 2: Nucleophilic attack by the tert-
butoxide ion on the isopropyl chloride
O-t-Bu- + (CH3)2CHCI → (CH3)2CHO-t-Bu +
CI-
Transcribed Image Text:Step 1: Formation of the nucleophile -tert- butoxide ion NaO-t-Bu + H2O → Na+ + OH- + O-t-Bu Step 2: Nucleophilic attack by the tert- butoxide ion on the isopropyl chloride O-t-Bu- + (CH3)2CHCI → (CH3)2CHO-t-Bu + CI-
Expert Solution
trending now

Trending now

This is a popular solution!

steps

Step by step

Solved in 2 steps with 2 images

Blurred answer
Knowledge Booster
Carboxylic Acids and their Derivatives
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.