Explain the oxidation of alkenes in different situations with examples.

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(N/A) Bayer's test (Test for unsaturation):
$KMnO_4$ (Potassium permanganate) is a purple-coloured solution. When alkenes react with cold,dilute alkaline $KMnO_4$ solution,the purple colour disappears,and a vicinal diol is formed. This process is known as hydroxylation.
Example: $CH_2=CH_2 + H_2O + [O] \xrightarrow{dil. KMnO_4, 273K} CH_2(OH)-CH_2(OH)$ (Ethane$-1,2-$diol).
$(b)$ Oxidation with strong oxidizing agents:
When alkenes are treated with strong oxidizing agents like acidic $KMnO_4$ or $K_2Cr_2O_7$ at high temperatures,the double bond is cleaved to form ketones or carboxylic acids,depending on the structure of the alkene.
Example: $CH_3-CH=CH-CH_3 \xrightarrow{KMnO_4/H^+} 2CH_3COOH$ (Ethanoic acid).

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Give the increasing order of stability for the following alkenes based on their heat of hydrogenation $(\Delta H^o)$:
$(I) (CH_3)_2C = C(CH_3)_2$
$(II) CH_3CH_2CH_2CH = CH_2$
$(III) (CH_3)_2C = CHCH_3$
$(IV) CH_3CH_2C(CH_3) = CH_2$

$CH_3-C(CH_3)=CH-CH_3 \xrightarrow[KMnO_4/\Delta]{NaIO_4}$ Product will be

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What is the structure of the $2$-butenyl radical?

Explain the reactivity of alkenes towards electrophilic reagents.

The major product formed in the following reaction is :
$CH_3CH=CHCH(CH_3)_2 \xrightarrow{HBr}$

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