write the magor producb formed by the fo llow wng reactron, Assume that you have enough of each reagont/ Reactant to drive the veactrion bo Completiion. Assume bhet there i's protic wek up aloe as nece ssarg ). NaBHey OH 2. Ht
write the magor producb formed by the fo llow wng reactron, Assume that you have enough of each reagont/ Reactant to drive the veactrion bo Completiion. Assume bhet there i's protic wek up aloe as nece ssarg ). NaBHey OH 2. Ht
Chemistry
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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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Question
![**Problem Statement:**
Write the major product formed by the following reaction. Assume that you have enough of each reagent/reactant to drive the reaction to completion. Assume that there is a protic workup done as necessary.
**Reaction:**
\[ \text{(Reactant)} \]
\[
\begin{array}{c}
\quad \quad \quad\quad
\begin{array}{ccccc}
\quad O & \quad & \quad & O & \\
// & OH & \quad & // & \quad & \\
\left\backslash \right| & & \left| \right/ & & \left\backslash \right| & & & \left| \right/ &&\\
\end{array}
\quad \quad \quad \quad 1.\text{NaBH}_4 \\
\end{array}
\ \quad 2.\text{H}^+
\]
1. **Sodium Borohydride (NaBH₄)**
2. **Acidic Workup (H⁺)**
**Explanation:**
The provided reaction involves the reduction of a compound using Sodium Borohydride (NaBH₄) followed by an acidic workup (H⁺). Sodium Borohydride is a common reagent for the reduction of ketones, aldehydes, and esters. In this case, it will likely reduce the carbonyl group (C=O) to an alcohol (C-OH). The exact structure of the product will depend on the specific details of the reactants and conditions but assuming standard behavior of NaBH₄, the reaction generally converts carbonyl functionalities to their corresponding alcohols.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F958545f1-0e13-4b00-b268-2dcd52627fd1%2F2fdec378-2c8f-4a10-a71e-fe0e1c6ab246%2Frfqyv6_processed.jpeg&w=3840&q=75)
Transcribed Image Text:**Problem Statement:**
Write the major product formed by the following reaction. Assume that you have enough of each reagent/reactant to drive the reaction to completion. Assume that there is a protic workup done as necessary.
**Reaction:**
\[ \text{(Reactant)} \]
\[
\begin{array}{c}
\quad \quad \quad\quad
\begin{array}{ccccc}
\quad O & \quad & \quad & O & \\
// & OH & \quad & // & \quad & \\
\left\backslash \right| & & \left| \right/ & & \left\backslash \right| & & & \left| \right/ &&\\
\end{array}
\quad \quad \quad \quad 1.\text{NaBH}_4 \\
\end{array}
\ \quad 2.\text{H}^+
\]
1. **Sodium Borohydride (NaBH₄)**
2. **Acidic Workup (H⁺)**
**Explanation:**
The provided reaction involves the reduction of a compound using Sodium Borohydride (NaBH₄) followed by an acidic workup (H⁺). Sodium Borohydride is a common reagent for the reduction of ketones, aldehydes, and esters. In this case, it will likely reduce the carbonyl group (C=O) to an alcohol (C-OH). The exact structure of the product will depend on the specific details of the reactants and conditions but assuming standard behavior of NaBH₄, the reaction generally converts carbonyl functionalities to their corresponding alcohols.
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