CARBOXYLIC ACIDS
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ALDEHYDES, KETONES AND CARBOXYLIC ACID

28449 Most acidic among the given acids

1 $\begin{array}{*{20}{c}}
  {C{H_3} - CH - C{H_2} - COOH} \\ 
  {|\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,} \\ 
  {Cl\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,} 
\end{array}$
2 \(CH -CH -CH -COOH\)
3 $\begin{array}{*{20}{c}}
  {C{H_3} - C{H_2} - CH - COOH} \\ 
  {\,\,\,\,\,\,|\,} \\ 
  {\,\,\,\,\,\,Cl} 
\end{array}$
4 All are of equal strength
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28450 \(\,\)

1 824-a973
2 824-b973
3 824-c973
4 824-d973
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28451 Which among the following compound is most acidic

1 824-a1047
2 824-b1047
3 824-c1047
4 824-d1047
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28452 \(2,\,2-\) Dimethylpropanoic acid on heating with sodalime gives

1 $\begin{array}{*{20}{c}}
  {\,\,\,\,\,C{H_3}} \\ 
  | \\ 
  {C{H_3} - C - C{H_3}} \\ 
  | \\ 
  {\,\,\,\,\,\,C{H_3}\,} 
\end{array}$
2 $\begin{array}{*{20}{c}}
  {\,\,\,\,\,\,\,C{H_3}\,} \\ 
  {|\,\,} \\ 
  {C{H_3} - C = C{H_2}} 
\end{array}$
3 $\begin{array}{*{20}{c}}
  {\,\,\,\,\,C{H_3}\,\,} \\ 
  {|\,\,\,\,\,\,} \\ 
  {C{H_3} - CH - C{H_3}} 
\end{array}$
4 $\begin{array}{*{20}{c}}
  {\,\,\,\,\,C{H_3}} \\ 
  | \\ 
  {C{H_3} - C - C{H_3}} \\ 
  | \\ 
  {\,\,\,\,\,\,OH\,} 
\end{array}$
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ALDEHYDES, KETONES AND CARBOXYLIC ACID

28449 Most acidic among the given acids

1 $\begin{array}{*{20}{c}}
  {C{H_3} - CH - C{H_2} - COOH} \\ 
  {|\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,} \\ 
  {Cl\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,} 
\end{array}$
2 \(CH -CH -CH -COOH\)
3 $\begin{array}{*{20}{c}}
  {C{H_3} - C{H_2} - CH - COOH} \\ 
  {\,\,\,\,\,\,|\,} \\ 
  {\,\,\,\,\,\,Cl} 
\end{array}$
4 All are of equal strength
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28450 \(\,\)

1 824-a973
2 824-b973
3 824-c973
4 824-d973
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28451 Which among the following compound is most acidic

1 824-a1047
2 824-b1047
3 824-c1047
4 824-d1047
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28452 \(2,\,2-\) Dimethylpropanoic acid on heating with sodalime gives

1 $\begin{array}{*{20}{c}}
  {\,\,\,\,\,C{H_3}} \\ 
  | \\ 
  {C{H_3} - C - C{H_3}} \\ 
  | \\ 
  {\,\,\,\,\,\,C{H_3}\,} 
\end{array}$
2 $\begin{array}{*{20}{c}}
  {\,\,\,\,\,\,\,C{H_3}\,} \\ 
  {|\,\,} \\ 
  {C{H_3} - C = C{H_2}} 
\end{array}$
3 $\begin{array}{*{20}{c}}
  {\,\,\,\,\,C{H_3}\,\,} \\ 
  {|\,\,\,\,\,\,} \\ 
  {C{H_3} - CH - C{H_3}} 
\end{array}$
4 $\begin{array}{*{20}{c}}
  {\,\,\,\,\,C{H_3}} \\ 
  | \\ 
  {C{H_3} - C - C{H_3}} \\ 
  | \\ 
  {\,\,\,\,\,\,OH\,} 
\end{array}$
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ALDEHYDES, KETONES AND CARBOXYLIC ACID

28449 Most acidic among the given acids

1 $\begin{array}{*{20}{c}}
  {C{H_3} - CH - C{H_2} - COOH} \\ 
  {|\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,} \\ 
  {Cl\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,} 
\end{array}$
2 \(CH -CH -CH -COOH\)
3 $\begin{array}{*{20}{c}}
  {C{H_3} - C{H_2} - CH - COOH} \\ 
  {\,\,\,\,\,\,|\,} \\ 
  {\,\,\,\,\,\,Cl} 
\end{array}$
4 All are of equal strength
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28450 \(\,\)

1 824-a973
2 824-b973
3 824-c973
4 824-d973
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28451 Which among the following compound is most acidic

1 824-a1047
2 824-b1047
3 824-c1047
4 824-d1047
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28452 \(2,\,2-\) Dimethylpropanoic acid on heating with sodalime gives

1 $\begin{array}{*{20}{c}}
  {\,\,\,\,\,C{H_3}} \\ 
  | \\ 
  {C{H_3} - C - C{H_3}} \\ 
  | \\ 
  {\,\,\,\,\,\,C{H_3}\,} 
\end{array}$
2 $\begin{array}{*{20}{c}}
  {\,\,\,\,\,\,\,C{H_3}\,} \\ 
  {|\,\,} \\ 
  {C{H_3} - C = C{H_2}} 
\end{array}$
3 $\begin{array}{*{20}{c}}
  {\,\,\,\,\,C{H_3}\,\,} \\ 
  {|\,\,\,\,\,\,} \\ 
  {C{H_3} - CH - C{H_3}} 
\end{array}$
4 $\begin{array}{*{20}{c}}
  {\,\,\,\,\,C{H_3}} \\ 
  | \\ 
  {C{H_3} - C - C{H_3}} \\ 
  | \\ 
  {\,\,\,\,\,\,OH\,} 
\end{array}$
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ALDEHYDES, KETONES AND CARBOXYLIC ACID

28449 Most acidic among the given acids

1 $\begin{array}{*{20}{c}}
  {C{H_3} - CH - C{H_2} - COOH} \\ 
  {|\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,} \\ 
  {Cl\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,} 
\end{array}$
2 \(CH -CH -CH -COOH\)
3 $\begin{array}{*{20}{c}}
  {C{H_3} - C{H_2} - CH - COOH} \\ 
  {\,\,\,\,\,\,|\,} \\ 
  {\,\,\,\,\,\,Cl} 
\end{array}$
4 All are of equal strength
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28450 \(\,\)

1 824-a973
2 824-b973
3 824-c973
4 824-d973
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28451 Which among the following compound is most acidic

1 824-a1047
2 824-b1047
3 824-c1047
4 824-d1047
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28452 \(2,\,2-\) Dimethylpropanoic acid on heating with sodalime gives

1 $\begin{array}{*{20}{c}}
  {\,\,\,\,\,C{H_3}} \\ 
  | \\ 
  {C{H_3} - C - C{H_3}} \\ 
  | \\ 
  {\,\,\,\,\,\,C{H_3}\,} 
\end{array}$
2 $\begin{array}{*{20}{c}}
  {\,\,\,\,\,\,\,C{H_3}\,} \\ 
  {|\,\,} \\ 
  {C{H_3} - C = C{H_2}} 
\end{array}$
3 $\begin{array}{*{20}{c}}
  {\,\,\,\,\,C{H_3}\,\,} \\ 
  {|\,\,\,\,\,\,} \\ 
  {C{H_3} - CH - C{H_3}} 
\end{array}$
4 $\begin{array}{*{20}{c}}
  {\,\,\,\,\,C{H_3}} \\ 
  | \\ 
  {C{H_3} - C - C{H_3}} \\ 
  | \\ 
  {\,\,\,\,\,\,OH\,} 
\end{array}$