Indirect hydration of an alkene cannot produce only one alcohol. This alcohol is $......$.

  • A
    $Ethyl \ alcohol$
  • B
    $Propyl \ alcohol$
  • C
    $Isobutyl \ alcohol$
  • D
    $Methyl \ alcohol$

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An alkene $A$ (molecular formula $C_{5}H_{10}$) on ozonolysis gives a mixture of two compounds $B$ and $C$. Compound $B$ gives a positive Fehling's test and also forms iodoform on treatment with $I_{2}$ and $NaOH$. Compound $C$ does not give Fehling's test but forms iodoform. Identify the compounds $A, B$ and $C$. Write the reaction for ozonolysis and the formation of iodoform from $B$ and $C$.

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Find out the major products $A$ and $B$ from the following reactions.

In the following reaction: $CH_3-C(CH_3)_2-CH=CH_2 \xrightarrow{H_2O/H^{+}} A + B$,the major product is:

$I$. $(CH_3)_2 C=CH_2 \xrightarrow{KMnO_4 / H^{+}} X + CO_2 + H_2 O$
$II$. $CH_3-CH=CH-CH_3 \xrightarrow{KMnO_4 / H^{+}} Y$
The functional groups in $X$ and $Y$ are respectively

Which of the following alkenes does $\underline{NOT}$ exhibit cis-trans isomerism?

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