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ALCOHOLS, PHENOLS AND ETHER

15432 The major organic product in the reaction is$CH_3 - O - CH(CH_3)_2 + HI \to$ products

1 $CH_3I + (CH_3)_2CHOH$

2 $CH_3OH + (CH_3)_2CHI$

3 $ICH_2OCH(CH_3)_2$

4 $\begin{array}{*{20}{c}}
{C{H_3}OC{{(C{H_3})}_2}} \\
|\,\,\, \\
I\,\,\,\,
\end{array}$

ALCOHOLS, PHENOLS AND ETHER

15433 $HBr$ reacts with $CH_2= CH - OCH_3$ under anhydrous conditions at room temperature to give

1 $BrCH_2- CH_2 - OCH_3$

2 $H_3C- CHBr - OCH_3$

3 $CH_3CHO$ and $CH_3Br$

4 $BrCH_2CHO$ and $CH_3OH$

ALCOHOLS, PHENOLS AND ETHER

15434 Among the following the one that gives positive iodoform test upon reaction with $I_2$ and $NaOH$ is

1 $\begin{array}{*{20}{c}}
{C{H_3}} \\
{|\,\,\,\,\,\,\,} \\
{C{H_3} - CHC{H_2}OH}
\end{array}$

2 $PhCHOHCH_3$

3 $CH_3CH_2CH(OH)CH_2CH_3$

4 $C_6H_5CH_2OH$

ALCOHOLS, PHENOLS AND ETHER

15435 The structure of the compound that gives a tribromo derivative on treatment with bromine water is

1

2

3

4

ALCOHOLS, PHENOLS AND ETHER

15432 The major organic product in the reaction is$CH_3 - O - CH(CH_3)_2 + HI \to$ products

1 $CH_3I + (CH_3)_2CHOH$

2 $CH_3OH + (CH_3)_2CHI$

3 $ICH_2OCH(CH_3)_2$

4 $\begin{array}{*{20}{c}}
{C{H_3}OC{{(C{H_3})}_2}} \\
|\,\,\, \\
I\,\,\,\,
\end{array}$

ALCOHOLS, PHENOLS AND ETHER

15433 $HBr$ reacts with $CH_2= CH - OCH_3$ under anhydrous conditions at room temperature to give

1 $BrCH_2- CH_2 - OCH_3$

2 $H_3C- CHBr - OCH_3$

3 $CH_3CHO$ and $CH_3Br$

4 $BrCH_2CHO$ and $CH_3OH$

ALCOHOLS, PHENOLS AND ETHER

15434 Among the following the one that gives positive iodoform test upon reaction with $I_2$ and $NaOH$ is

1 $\begin{array}{*{20}{c}}
{C{H_3}} \\
{|\,\,\,\,\,\,\,} \\
{C{H_3} - CHC{H_2}OH}
\end{array}$

2 $PhCHOHCH_3$

3 $CH_3CH_2CH(OH)CH_2CH_3$

4 $C_6H_5CH_2OH$

ALCOHOLS, PHENOLS AND ETHER

15435 The structure of the compound that gives a tribromo derivative on treatment with bromine water is

1

2

3

4

ALCOHOLS, PHENOLS AND ETHER

15432 The major organic product in the reaction is$CH_3 - O - CH(CH_3)_2 + HI \to$ products

1 $CH_3I + (CH_3)_2CHOH$

2 $CH_3OH + (CH_3)_2CHI$

3 $ICH_2OCH(CH_3)_2$

4 $\begin{array}{*{20}{c}}
{C{H_3}OC{{(C{H_3})}_2}} \\
|\,\,\, \\
I\,\,\,\,
\end{array}$

ALCOHOLS, PHENOLS AND ETHER

15433 $HBr$ reacts with $CH_2= CH - OCH_3$ under anhydrous conditions at room temperature to give

1 $BrCH_2- CH_2 - OCH_3$

2 $H_3C- CHBr - OCH_3$

3 $CH_3CHO$ and $CH_3Br$

4 $BrCH_2CHO$ and $CH_3OH$

ALCOHOLS, PHENOLS AND ETHER

15434 Among the following the one that gives positive iodoform test upon reaction with $I_2$ and $NaOH$ is

1 $\begin{array}{*{20}{c}}
{C{H_3}} \\
{|\,\,\,\,\,\,\,} \\
{C{H_3} - CHC{H_2}OH}
\end{array}$

2 $PhCHOHCH_3$

3 $CH_3CH_2CH(OH)CH_2CH_3$

4 $C_6H_5CH_2OH$

ALCOHOLS, PHENOLS AND ETHER

15435 The structure of the compound that gives a tribromo derivative on treatment with bromine water is

1

2

3

4

ALCOHOLS, PHENOLS AND ETHER

15432 The major organic product in the reaction is$CH_3 - O - CH(CH_3)_2 + HI \to$ products

1 $CH_3I + (CH_3)_2CHOH$

2 $CH_3OH + (CH_3)_2CHI$

3 $ICH_2OCH(CH_3)_2$

4 $\begin{array}{*{20}{c}}
{C{H_3}OC{{(C{H_3})}_2}} \\
|\,\,\, \\
I\,\,\,\,
\end{array}$

ALCOHOLS, PHENOLS AND ETHER

15433 $HBr$ reacts with $CH_2= CH - OCH_3$ under anhydrous conditions at room temperature to give

1 $BrCH_2- CH_2 - OCH_3$

2 $H_3C- CHBr - OCH_3$

3 $CH_3CHO$ and $CH_3Br$

4 $BrCH_2CHO$ and $CH_3OH$

ALCOHOLS, PHENOLS AND ETHER

15434 Among the following the one that gives positive iodoform test upon reaction with $I_2$ and $NaOH$ is

1 $\begin{array}{*{20}{c}}
{C{H_3}} \\
{|\,\,\,\,\,\,\,} \\
{C{H_3} - CHC{H_2}OH}
\end{array}$

2 $PhCHOHCH_3$

3 $CH_3CH_2CH(OH)CH_2CH_3$

4 $C_6H_5CH_2OH$

ALCOHOLS, PHENOLS AND ETHER

15435 The structure of the compound that gives a tribromo derivative on treatment with bromine water is

1

2

3

4

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