The image displays a chemistry problem that asks to draw the product of a reaction. It specifically mentions to "ignore inorganic byproducts." The given reactant is a cyclopentanone structure, identified by a five-membered ring with a double-bonded oxygen (a ketone group) and a hydrogen attached to the carbonyl carbon. Below the structure, the reagents are specified as:- NaBH₄ (sodium borohydride)- CH₃CH₂OH (ethanol)An arrow pointing downwards indicates that these reagents will be used to reduce the reactant. A dashed box labeled "Drawing" suggests where the user is expected to draw the reaction product. Sodium borohydride is commonly used as a reducing agent, converting ketones to secondary alcohols. Therefore, the expected product will likely be cyclopentanol, with the carbonyl group reduced to a hydroxyl group.

Given is organic reaction. NaBH4 is mild reducing agent which reduces ketone to secondary alcohol…

Answered: byproducts. NaBH4 CH3CH₂OH elow. Ignore…

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byproducts. NaBH4 CH3CH₂OH elow. Ignore inorganic H O Q Atoms, and R Draw or ta

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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Question

The image displays a chemistry problem that asks to draw the product of a reaction. It specifically mentions to "ignore inorganic byproducts." The given reactant is a cyclopentanone structure, identified by a five-membered ring with a double-bonded oxygen (a ketone group) and a hydrogen attached to the carbonyl carbon.

Below the structure, the reagents are specified as:
- NaBH₄ (sodium borohydride)
- CH₃CH₂OH (ethanol)

An arrow pointing downwards indicates that these reagents will be used to reduce the reactant. A dashed box labeled "Drawing" suggests where the user is expected to draw the reaction product.

Sodium borohydride is commonly used as a reducing agent, converting ketones to secondary alcohols. Therefore, the expected product will likely be cyclopentanol, with the carbonyl group reduced to a hydroxyl group.

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