**Title:** Predicting Major Products in Organic Reactions**Question:** Predict the major product(s) for each of the following reactions:**Reaction Scheme:**1. **Starting Compound:** A cyclic ester (lactone) structure comprised of a six-membered ring with two oxygen atoms; one in the ring and one as a carbonyl group.2. **Reagents:** - Step 1: Phenylmagnesium Bromide (PhMgBr) - Step 2: Aqueous Acid (H₃O⁺)**Expected Products:**- The reaction involves a nucleophilic addition of phenylmagnesium bromide (a Grignard reagent) to the carbonyl group of the lactone. Following the addition, hydrolysis with aqueous acid leads to a ring opening and the formation of an alcohol. - The product shown is a compound featuring: - A phenyl group attached to what was previously the carbonyl carbon. - An open chain with a hydroxyl (OH) group indicating alcohol formation.This transformation is typical of Grignard additions to esters and lactones, yielding tertiary alcohols via nucleophilic acyl substitution followed by hydrolysis.

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Predict the major product(s) for each of the following: [3 1) PhMgBr 2) H₂O* ?

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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