Propose structures for hydrocarbons that give the following products on oxidative cleavage by $K M n O_{4}$ or $O_{3}$ :
$H O O C (C H_{2})_{8} C O O H$

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Solution

The correct option is A
Non-terminal alkynes, on oxidative cleavage yield carboxylic acids.
Lack of symmetry around the triple bond would yield a mixture of acids.

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Propose structures for hydrocarbons that give the following products on oxidative cleavage by $K M n O_{4}$ or $O_{3}$ :
$H O O C (C H_{2})_{8} C O O H$

Q. Propose structures for hydrocarbons that give the following products on oxidative cleavage by

K M n O_{4}

O_{3}

Q. Propose structure/structures for the hydrocarbon that gives the following products on oxidative cleavage by

K M n O_{4} / H^{\oplus}

Q. Propose structures for the hydrocrbon that gives the following products on oxidative cleavage by

K M n O_{4} / H^{\oplus}

Q. Assertion :Treatment of one mole of

2

-butene with

O_{3}

followed by.work-up with

H_{2} O_{2}

gives

2

moles of acetic acid. Reason:

H_{2} O_{2}

bring about oxidative cleavage of intermediate cyanide.

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Propose structures for hydrocarbons that give the following products on oxidative cleavage by KMnO4 or O3: HOOC(CH2)8COOH

The correct option is A Non-terminal alkynes, on oxidative cleavage yield carboxylic acids. Lack of symmetry around the triple bond would yield a mixture of acids.

Propose structures for hydrocarbons that give the following products on oxidative cleavage by $K M n O_{4}$ or $O_{3}$ :
$H O O C (C H_{2})_{8} C O O H$

The correct option is A
Non-terminal alkynes, on oxidative cleavage yield carboxylic acids.
Lack of symmetry around the triple bond would yield a mixture of acids.