To describe the method of synthesis of butanone in a high yield from butane. Concept introduction: Butane can be converted to butanone by first halogenating it because alkanes easily undergo halogenation. The halogenated product undergoes basic hydrolysis, the product formed is oxidized to form the corresponding ketone that is butanone. Halogenation can take place with either chlorine or bromine but bromine is preferred because it is more selective than chlorine. The structural formula for butane is: The structural formula for butanone is:

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Answer 1

Question

Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 15, Problem 64P

Interpretation Introduction

Interpretation:

To describe the method of synthesis of butanone in a high yield from butane.

Concept introduction:

Butane can be converted to butanone by first halogenating it because alkanes easily undergo halogenation. The halogenated product undergoes basic hydrolysis, the product formed is oxidized to form the corresponding ketone that is butanone.

Halogenation can take place with either chlorine or bromine but bromine is preferred because it is more selective than chlorine.

The structural formula for butane is:

The structural formula for butanone is:

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What is the missing reactant in this organic reaction? + R -A HO IN + H₂O Specifically, in the drawing area below draw the skeletal ("line") structure of R. If there is more than one reasonable answer, you can draw any one of them. If there is no reasonable answer, check the No answer box under the drawing area. Note for advanced students: you may assume no products other than those shown above are formed. Explanation Check Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center

Stuc X ctclix ALE X A ALE אן A ALEX Lab (195 X Nut x M Inb x NU X NUT X Unt x + → C www-awu.aleks.com/alekscgi/x/Isl.exe/10_u-lgNslkr7j8P3jH-IQ1g8NUi-mObKa_ZLx2twjEhK7mVG6PulJI006NcKTV37JxMpZuyrVCdQolLAKqp_7U3r1GUD3... New Chrome available: Naomi Question 26 of 39 (4 points) | Question Attempt: 1 of Unlimited Give the IUPAC name. 2,3-dimethylhexane Part: 1/2 Part 2 of 2 Draw the skeletal structure of a constitutional isomer of the alkane above that contains a different number of carbons in its longest chain. Skip Part Check Click and drag to start drawing a structure. 3 Finance headline Q Search mwa Harvard Intensifi... X Save For Later 00 dlo HB Submit Assignment 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility a 9:11 PM 4/22/2025

Predict the product of this organic reaction: + NH2 HO A P+ H2O Specifically, in the drawing area below draw the skeletal ("line") structure of P. If there is no reasonable possibility for P, check the No answer box under the drawing area. Click and drag to start drawing a structure. ✓

Answer 2

Question

Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 15, Problem 64P

Interpretation Introduction

Interpretation:

To describe the method of synthesis of butanone in a high yield from butane.

Concept introduction:

Butane can be converted to butanone by first halogenating it because alkanes easily undergo halogenation. The halogenated product undergoes basic hydrolysis, the product formed is oxidized to form the corresponding ketone that is butanone.

Halogenation can take place with either chlorine or bromine but bromine is preferred because it is more selective than chlorine.

The structural formula for butane is:

The structural formula for butanone is:

Expert Solution & Answer

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Check out a sample textbook solution

See solution

Answer 3

Question

Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 15, Problem 64P

Interpretation Introduction

Interpretation:

To describe the method of synthesis of butanone in a high yield from butane.

Concept introduction:

Butane can be converted to butanone by first halogenating it because alkanes easily undergo halogenation. The halogenated product undergoes basic hydrolysis, the product formed is oxidized to form the corresponding ketone that is butanone.

Halogenation can take place with either chlorine or bromine but bromine is preferred because it is more selective than chlorine.

The structural formula for butane is:

The structural formula for butanone is:

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 15, Problem 64P

Interpretation Introduction