Which best describes the first step of the mechanism of the reaction below?+ CH₂MgBrH3C1) ether2) H3O+→CH3CH3MgBr acts as an nucleophile and attacks the carbonyl carbon.The carbonyl carbon acts as an nucleophile and attacks CH3MgBr.The methyl group on acetone leaves forming a carbonyl carbocation.O CH3MgBr acts as an electrophile and attacks the carbonyl oxygen.

Option 1st is correct: CH3MgBr acts as an nucleophile and attacks the carbonyl carbon.

Which best describes the first step of the mechanism of the reaction below? 0 .C H3C + CH₂MgBr 1) ether 2) H3O+ CH3 CH3MgBr acts as an nucleophile and attacks the carbonyl carbon. O The carbonyl carbon acts as an nucleophile and attacks CH3MgBr. O The methyl group on acetone leaves forming a carbonyl carbocation. O CH3MgBr acts as an electrophile and attacks the carbonyl oxygen.

Which best describes the first step of the mechanism of the reaction below? 0 .C H3C + CH₂MgBr 1) ether 2) H3O+ CH3 CH3MgBr acts as an nucleophile and attacks the carbonyl carbon. O The carbonyl carbon acts as an nucleophile and attacks CH3MgBr. O The methyl group on acetone leaves forming a carbonyl carbocation. O CH3MgBr acts as an electrophile and attacks the carbonyl oxygen.

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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