**Synthesis Reagent Selection Exercise**In this exercise, you are tasked with determining the appropriate reagent for each step of the following organic synthesis. The starting material is an alcohol, and the final product is a secondary alcohol with a phenyl group.**Reaction Steps:**- **Step 1:** Conversion of an alcohol to a compound intermediate.- **Step 2:** Formation of a secondary alcohol with a phenyl group.**Reagents Available:**a. LiAlH₄ b. H₂SO₄ c. HCl d. HBr e. SOCl₂ f. PBr₃ g. Dess-Martin periodinane (DMP) h. NaH i. NaOH j. CH₃MgBr k. CH₃CH₂MgBr l. C₆H₅MgBr (phenylmagnesium bromide) m. (CH₃)₂CHMgBr n. CrO₃ **Instructions:**Write the letter(s) of the reagent(s) you would use for each step in the synthesis boxes below.- **Reagent for Step 1:** [ ]- **Reagent for Step 2:** [ ]**Note:** Evaluate the transformation in each step and utilize your knowledge of organic chemistry reactions to pair the correct reagent with each step.

A question based on reactions to alcohol. A primary alcohol reagent and the final product are given the interim product and the respective reagents are to be determined.Primary alcohol can be converted into the respective aldehyde by mild oxidation. Aldehyde can be converted into secondary alcohol by the reaction with Grignard reagent.AnswerReagent for the step 1: nReagent for the step 2: lComplete equation

Answered: Specify the reagent you would use in…

Science

Chemistry

Specify the reagent you would use in each step of the following synthesis: OH step 1 step 2 OH

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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