The product formed in the following chemical reaction is:





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:
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.
The reaction sequence given below is carried out with 16 moles of X. The yield of the major product in each step is given below the product in parentheses. The amount (in grams) of S produced is ____. 
Use: Atomic mass (in amu): H = 1, C = 12, O = 16, Br = 80
A sphere of radius R is cut from a larger solid sphere of radius 2R as shown in the figure. The ratio of the moment of inertia of the smaller sphere to that of the rest part of the sphere about the Y-axis is : 
A constant voltage of 50 V is maintained between the points A and B of the circuit shown in the figure. The current through the branch CD of the circuit is :
The current passing through the battery in the given circuit, is: 
Given below are two statements:
Statement I: The primary source of energy in an ecosystem is solar energy.
Statement II: The rate of production of organic matter during photosynthesis in an ecosystem is called net primary productivity (NPP).
In light of the above statements, choose the most appropriate answer from the options given below:
SN1 reaction mechanism takes place by following three steps –
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.
The mechanism of an electrophilic aromatic substitution reaction contains three main components which are:
The electrophilic substitution reaction mechanism is composed of three steps, which will be discussed more below.