Question:

The product formed in the following chemical reaction is:

chemical reaction

Updated On: Nov 13, 2025
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The Correct Option is A

Solution and Explanation

To determine the product formed in the given chemical reaction, we need to analyze the reaction conditions and the given compound.

The reaction involves the reduction of a keto group using sodium borohydride (\( \text{NaBH}_4 \)) in ethanol (\( \text{C}_2\text{H}_5\text{OH} \)). Sodium borohydride is a selective reducing agent that primarily reduces aldehydes and ketones to alcohols.

The structure of the reactant is given as:

In this compound, the carbonyl group (C=O) is present as a ketone. Sodium borohydride will reduce this ketone group to a secondary alcohol by adding hydrogen across the C=O bond.

Let's analyze what the product will look like:

  1. The carbonyl group (C=O) gets reduced to a hydroxyl group (C-OH).
  2. The rest of the compound remains unchanged as NaBH4 is a selective reducing agent and does not alter other functional groups in this context.

Hence, the ketone is reduced to a secondary alcohol.

Therefore, the product of the reaction is:

This is the correct answer because it shows the formation of a secondary alcohol from the reduction of the ketone group.

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Concepts Used:

Organic Chemistry – Some Basic Principles and Techniques - Reaction Mechanism

SN1 Reaction Mechanism:

SN1 reaction mechanism takes place by following three steps –

  • Formation of carbocation 
  • Attack of nucleophile 
  • Deprotonation 

SN2 Reaction Mechanism:

The SN2 reaction mechanism involves the nucleophilic substitution reaction of the leaving group (which generally consists of halide groups or other electron-withdrawing groups) with a nucleophile in a given organic compound.

Electrophilic Aromatic Substitution Reaction Mechanism:

The mechanism of an electrophilic aromatic substitution reaction contains three main components which are:

  1. A new sigma bond from C=C is formed during the reaction in the arene nucleophile.
  2. Due to the breaking of the C-H sigma bond, a proton is removed.
  3. The C=C bond is reformed and it restores the aromaticity of the compound.

Electrophilic Substitution Reaction Mechanism:

The electrophilic substitution reaction mechanism is composed of three steps, which will be discussed more below.

  • Electrophile Generation
  • Carbocation Formation
  • Proton Removal