What is a key difference between the following two reactions?CH,MgBrCH,NH2a) CH3MgBr would deprotonate the alpha position and CH3NH2 would adddirectly to the C=Ob) CH3MGB would deprotonate the alpha position and CH3NH2 would add inthe beta positionO c) CH3MgBr would add directly to the C=O and CH3NH2 would add in the betapositionO d) CH3M¤B would add in the beta position and CH3NH2 would add directly tothe C=O What substrates are needed to synthesize the Robinson annulation product below?PhPh.Ph.3a) 1 and 3O b) 2 and 3O c) 1 and 4d) 2 and 4

The question is based on the concept of organic reactions. we have to identify the Product formed…

hat is a key difference between the following two reactions? CH,MgBr CH,NH2 a) CH3MgBr would deprotonate the alpha position and CH3NH2 would add directly to the C=o ) b) CH3MgBr would deprotonate the alpha position and CH3NH2 would add in the beta position c) CH3MgBr would add directly to the C=O and CH3NH2 would add in the beta position d) CH3MBB would add in the beta position and CH3NH2 would add directly to the C=O

hat is a key difference between the following two reactions? CH,MgBr CH,NH2 a) CH3MgBr would deprotonate the alpha position and CH3NH2 would add directly to the C=o ) b) CH3MgBr would deprotonate the alpha position and CH3NH2 would add in the beta position c) CH3MgBr would add directly to the C=O and CH3NH2 would add in the beta position d) CH3MBB would add in the beta position and CH3NH2 would add directly to the C=O

Fundamentals Of Analytical Chemistry

9th Edition

ISBN:9781285640686

Author:Skoog

Publisher:Skoog

Chapter30: Kinetic Methods Of Analysis

Section: Chapter Questions

Problem 30.15QAP

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