Aromatic Hydrocarbon
CHXI13:HYDROCARBONS

318275 When benzene diazonium chloride is treated with \(\mathrm{H}_{3} \mathrm{PO}_{2}\), the product formed is

1 toluene
2 phenol
3 benzene
4 benzaldehyde
CHXI13:HYDROCARBONS

318276 \({{\text{C}}_{\text{6}}}{{\text{H}}_{\text{6}}} + {\text{CC}}{{\text{l}}_{\text{4}}}\xrightarrow{{{\text{AlC}}{{\text{l}}_{\text{3}}}}}{\text{X}}\xrightarrow{{{{\text{H}}_{\text{2}}}{\text{O}}}}{\text{Z}}\) The product Z is

1 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{COOH}\)
2 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CHO}\)
3 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CCl}_{2} \mathrm{C}_{6} \mathrm{H}_{5}\)
4 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{COC}_{6} \mathrm{H}_{5}\)
CHXI13:HYDROCARBONS

318277 In the following sequence of reactions
\({\text{Toluene }}\xrightarrow{{{\text{KMn}}{{\text{O}}_{\text{4}}}}}{\text{A}}\,\xrightarrow{{{\text{SOC}}{{\text{l}}_{\text{2}}}}}{\text{B}}\,\xrightarrow[{{\text{BaS}}{{\text{O}}_{\text{4}}}}]{{{{\text{H}}_{\text{2}}}{\text{/Pd}}}}{\text{C}}{\text{.}}\) The product \(\mathrm{C}\) is

1 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CH}_{2} \mathrm{OH}\)
2 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CHO}\)
3 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{COOH}\)
4 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CH}_{3}\)
CHXI13:HYDROCARBONS

318278 The compound formed as a result of oxidation of ethyl benzene by \(\mathrm{KMnO}_{4}\) is

1 Benzyl alcohol
2 Benzophenone
3 Acetophenone
4 Benzoic acid
CHXI13:HYDROCARBONS

318275 When benzene diazonium chloride is treated with \(\mathrm{H}_{3} \mathrm{PO}_{2}\), the product formed is

1 toluene
2 phenol
3 benzene
4 benzaldehyde
CHXI13:HYDROCARBONS

318276 \({{\text{C}}_{\text{6}}}{{\text{H}}_{\text{6}}} + {\text{CC}}{{\text{l}}_{\text{4}}}\xrightarrow{{{\text{AlC}}{{\text{l}}_{\text{3}}}}}{\text{X}}\xrightarrow{{{{\text{H}}_{\text{2}}}{\text{O}}}}{\text{Z}}\) The product Z is

1 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{COOH}\)
2 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CHO}\)
3 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CCl}_{2} \mathrm{C}_{6} \mathrm{H}_{5}\)
4 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{COC}_{6} \mathrm{H}_{5}\)
CHXI13:HYDROCARBONS

318277 In the following sequence of reactions
\({\text{Toluene }}\xrightarrow{{{\text{KMn}}{{\text{O}}_{\text{4}}}}}{\text{A}}\,\xrightarrow{{{\text{SOC}}{{\text{l}}_{\text{2}}}}}{\text{B}}\,\xrightarrow[{{\text{BaS}}{{\text{O}}_{\text{4}}}}]{{{{\text{H}}_{\text{2}}}{\text{/Pd}}}}{\text{C}}{\text{.}}\) The product \(\mathrm{C}\) is

1 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CH}_{2} \mathrm{OH}\)
2 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CHO}\)
3 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{COOH}\)
4 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CH}_{3}\)
CHXI13:HYDROCARBONS

318278 The compound formed as a result of oxidation of ethyl benzene by \(\mathrm{KMnO}_{4}\) is

1 Benzyl alcohol
2 Benzophenone
3 Acetophenone
4 Benzoic acid
CHXI13:HYDROCARBONS

318275 When benzene diazonium chloride is treated with \(\mathrm{H}_{3} \mathrm{PO}_{2}\), the product formed is

1 toluene
2 phenol
3 benzene
4 benzaldehyde
CHXI13:HYDROCARBONS

318276 \({{\text{C}}_{\text{6}}}{{\text{H}}_{\text{6}}} + {\text{CC}}{{\text{l}}_{\text{4}}}\xrightarrow{{{\text{AlC}}{{\text{l}}_{\text{3}}}}}{\text{X}}\xrightarrow{{{{\text{H}}_{\text{2}}}{\text{O}}}}{\text{Z}}\) The product Z is

1 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{COOH}\)
2 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CHO}\)
3 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CCl}_{2} \mathrm{C}_{6} \mathrm{H}_{5}\)
4 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{COC}_{6} \mathrm{H}_{5}\)
CHXI13:HYDROCARBONS

318277 In the following sequence of reactions
\({\text{Toluene }}\xrightarrow{{{\text{KMn}}{{\text{O}}_{\text{4}}}}}{\text{A}}\,\xrightarrow{{{\text{SOC}}{{\text{l}}_{\text{2}}}}}{\text{B}}\,\xrightarrow[{{\text{BaS}}{{\text{O}}_{\text{4}}}}]{{{{\text{H}}_{\text{2}}}{\text{/Pd}}}}{\text{C}}{\text{.}}\) The product \(\mathrm{C}\) is

1 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CH}_{2} \mathrm{OH}\)
2 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CHO}\)
3 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{COOH}\)
4 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CH}_{3}\)
CHXI13:HYDROCARBONS

318278 The compound formed as a result of oxidation of ethyl benzene by \(\mathrm{KMnO}_{4}\) is

1 Benzyl alcohol
2 Benzophenone
3 Acetophenone
4 Benzoic acid
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CHXI13:HYDROCARBONS

318275 When benzene diazonium chloride is treated with \(\mathrm{H}_{3} \mathrm{PO}_{2}\), the product formed is

1 toluene
2 phenol
3 benzene
4 benzaldehyde
CHXI13:HYDROCARBONS

318276 \({{\text{C}}_{\text{6}}}{{\text{H}}_{\text{6}}} + {\text{CC}}{{\text{l}}_{\text{4}}}\xrightarrow{{{\text{AlC}}{{\text{l}}_{\text{3}}}}}{\text{X}}\xrightarrow{{{{\text{H}}_{\text{2}}}{\text{O}}}}{\text{Z}}\) The product Z is

1 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{COOH}\)
2 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CHO}\)
3 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CCl}_{2} \mathrm{C}_{6} \mathrm{H}_{5}\)
4 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{COC}_{6} \mathrm{H}_{5}\)
CHXI13:HYDROCARBONS

318277 In the following sequence of reactions
\({\text{Toluene }}\xrightarrow{{{\text{KMn}}{{\text{O}}_{\text{4}}}}}{\text{A}}\,\xrightarrow{{{\text{SOC}}{{\text{l}}_{\text{2}}}}}{\text{B}}\,\xrightarrow[{{\text{BaS}}{{\text{O}}_{\text{4}}}}]{{{{\text{H}}_{\text{2}}}{\text{/Pd}}}}{\text{C}}{\text{.}}\) The product \(\mathrm{C}\) is

1 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CH}_{2} \mathrm{OH}\)
2 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CHO}\)
3 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{COOH}\)
4 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CH}_{3}\)
CHXI13:HYDROCARBONS

318278 The compound formed as a result of oxidation of ethyl benzene by \(\mathrm{KMnO}_{4}\) is

1 Benzyl alcohol
2 Benzophenone
3 Acetophenone
4 Benzoic acid