Alkenes
NEET Test Series from KOTA - 10 Papers In MS WORD WhatsApp Here
CHXI13:HYDROCARBONS

318066 In the following sequence of reactions, the compound ' \(\mathrm{A}\) ' is
\({\text{A}}\xrightarrow{{{\text{HBr}}}}{\text{B}}\xrightarrow{{{\text{Alc}}{\text{.KOH}}}}{\text{C}}\xrightarrow{{{{\text{O}}_{\text{3}}}{\text{,Zn/}}{{\text{H}}_{\text{2}}}{\text{O}}}}\)
\({\text{C}}{{\text{H}}_{\text{3}}}{\text{CHO + HCHO}}\)

1 Ethylene
2 Acetic acid
3 Propene
4 1-Butene
CHXI13:HYDROCARBONS

318067 \(\mathop {{{\text{C}}_{\text{3}}}{{\text{H}}_{\text{7}}}{\text{Cl}}}\limits_{\left[ {\text{A}} \right]} \xrightarrow[{{\text{KOH}}}]{{{\text{alc}}}}\left[ {\text{B}} \right]\xrightarrow{{{\text{HCl}}}}\left[ {\text{C}} \right]\xrightarrow[{{\text{KOH}}}]{{{\text{(aq)}}}}\mathop {{{\text{C}}_{\text{3}}}{{\text{H}}_{\text{8}}}{\text{O}}}\limits_{\left[ {\text{D}} \right]} \)
The compound " A " is

1 1-Chloro propane
2 2-Chloro propane
3 Both of these
4 None of these
CHXI13:HYDROCARBONS

318068 The final solution left after kolbe's electrolysis in the manufacutre of ethene is

1 Alkaline
2 Acidic
3 Neutral
4 Cant be predicted.
CHXI13:HYDROCARBONS

318069 An alkyl chloride (A) produces a single alkene on reaction with sodium ethoxide and ethanol. The alkene further undergoes hydrogenation to yield 2-methylbutane. The alkyl chloride (A) is

1 \(\mathrm{ClCH}_{2} \mathrm{C}\left(\mathrm{CH}_{3}\right)_{3}\)
2 \(\mathrm{ClCH}_{2} \mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{CH}_{3}\)
3 \(\mathrm{ClCH}_{2} \mathrm{CH}\left(\mathrm{CH}_{3}\right) \mathrm{CH}_{2} \mathrm{CH}_{3}\)
4 \(\mathrm{CH}_{3} \mathrm{C}(\mathrm{Cl})\left(\mathrm{CH}_{3}\right) \mathrm{CH}_{2} \mathrm{CH}_{3}\)
CHXI13:HYDROCARBONS

318066 In the following sequence of reactions, the compound ' \(\mathrm{A}\) ' is
\({\text{A}}\xrightarrow{{{\text{HBr}}}}{\text{B}}\xrightarrow{{{\text{Alc}}{\text{.KOH}}}}{\text{C}}\xrightarrow{{{{\text{O}}_{\text{3}}}{\text{,Zn/}}{{\text{H}}_{\text{2}}}{\text{O}}}}\)
\({\text{C}}{{\text{H}}_{\text{3}}}{\text{CHO + HCHO}}\)

1 Ethylene
2 Acetic acid
3 Propene
4 1-Butene
CHXI13:HYDROCARBONS

318067 \(\mathop {{{\text{C}}_{\text{3}}}{{\text{H}}_{\text{7}}}{\text{Cl}}}\limits_{\left[ {\text{A}} \right]} \xrightarrow[{{\text{KOH}}}]{{{\text{alc}}}}\left[ {\text{B}} \right]\xrightarrow{{{\text{HCl}}}}\left[ {\text{C}} \right]\xrightarrow[{{\text{KOH}}}]{{{\text{(aq)}}}}\mathop {{{\text{C}}_{\text{3}}}{{\text{H}}_{\text{8}}}{\text{O}}}\limits_{\left[ {\text{D}} \right]} \)
The compound " A " is

1 1-Chloro propane
2 2-Chloro propane
3 Both of these
4 None of these
CHXI13:HYDROCARBONS

318068 The final solution left after kolbe's electrolysis in the manufacutre of ethene is

1 Alkaline
2 Acidic
3 Neutral
4 Cant be predicted.
CHXI13:HYDROCARBONS

318069 An alkyl chloride (A) produces a single alkene on reaction with sodium ethoxide and ethanol. The alkene further undergoes hydrogenation to yield 2-methylbutane. The alkyl chloride (A) is

1 \(\mathrm{ClCH}_{2} \mathrm{C}\left(\mathrm{CH}_{3}\right)_{3}\)
2 \(\mathrm{ClCH}_{2} \mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{CH}_{3}\)
3 \(\mathrm{ClCH}_{2} \mathrm{CH}\left(\mathrm{CH}_{3}\right) \mathrm{CH}_{2} \mathrm{CH}_{3}\)
4 \(\mathrm{CH}_{3} \mathrm{C}(\mathrm{Cl})\left(\mathrm{CH}_{3}\right) \mathrm{CH}_{2} \mathrm{CH}_{3}\)
CHXI13:HYDROCARBONS

318066 In the following sequence of reactions, the compound ' \(\mathrm{A}\) ' is
\({\text{A}}\xrightarrow{{{\text{HBr}}}}{\text{B}}\xrightarrow{{{\text{Alc}}{\text{.KOH}}}}{\text{C}}\xrightarrow{{{{\text{O}}_{\text{3}}}{\text{,Zn/}}{{\text{H}}_{\text{2}}}{\text{O}}}}\)
\({\text{C}}{{\text{H}}_{\text{3}}}{\text{CHO + HCHO}}\)

1 Ethylene
2 Acetic acid
3 Propene
4 1-Butene
CHXI13:HYDROCARBONS

318067 \(\mathop {{{\text{C}}_{\text{3}}}{{\text{H}}_{\text{7}}}{\text{Cl}}}\limits_{\left[ {\text{A}} \right]} \xrightarrow[{{\text{KOH}}}]{{{\text{alc}}}}\left[ {\text{B}} \right]\xrightarrow{{{\text{HCl}}}}\left[ {\text{C}} \right]\xrightarrow[{{\text{KOH}}}]{{{\text{(aq)}}}}\mathop {{{\text{C}}_{\text{3}}}{{\text{H}}_{\text{8}}}{\text{O}}}\limits_{\left[ {\text{D}} \right]} \)
The compound " A " is

1 1-Chloro propane
2 2-Chloro propane
3 Both of these
4 None of these
CHXI13:HYDROCARBONS

318068 The final solution left after kolbe's electrolysis in the manufacutre of ethene is

1 Alkaline
2 Acidic
3 Neutral
4 Cant be predicted.
CHXI13:HYDROCARBONS

318069 An alkyl chloride (A) produces a single alkene on reaction with sodium ethoxide and ethanol. The alkene further undergoes hydrogenation to yield 2-methylbutane. The alkyl chloride (A) is

1 \(\mathrm{ClCH}_{2} \mathrm{C}\left(\mathrm{CH}_{3}\right)_{3}\)
2 \(\mathrm{ClCH}_{2} \mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{CH}_{3}\)
3 \(\mathrm{ClCH}_{2} \mathrm{CH}\left(\mathrm{CH}_{3}\right) \mathrm{CH}_{2} \mathrm{CH}_{3}\)
4 \(\mathrm{CH}_{3} \mathrm{C}(\mathrm{Cl})\left(\mathrm{CH}_{3}\right) \mathrm{CH}_{2} \mathrm{CH}_{3}\)
NEET Test Series from KOTA - 10 Papers In MS WORD WhatsApp Here
CHXI13:HYDROCARBONS

318066 In the following sequence of reactions, the compound ' \(\mathrm{A}\) ' is
\({\text{A}}\xrightarrow{{{\text{HBr}}}}{\text{B}}\xrightarrow{{{\text{Alc}}{\text{.KOH}}}}{\text{C}}\xrightarrow{{{{\text{O}}_{\text{3}}}{\text{,Zn/}}{{\text{H}}_{\text{2}}}{\text{O}}}}\)
\({\text{C}}{{\text{H}}_{\text{3}}}{\text{CHO + HCHO}}\)

1 Ethylene
2 Acetic acid
3 Propene
4 1-Butene
CHXI13:HYDROCARBONS

318067 \(\mathop {{{\text{C}}_{\text{3}}}{{\text{H}}_{\text{7}}}{\text{Cl}}}\limits_{\left[ {\text{A}} \right]} \xrightarrow[{{\text{KOH}}}]{{{\text{alc}}}}\left[ {\text{B}} \right]\xrightarrow{{{\text{HCl}}}}\left[ {\text{C}} \right]\xrightarrow[{{\text{KOH}}}]{{{\text{(aq)}}}}\mathop {{{\text{C}}_{\text{3}}}{{\text{H}}_{\text{8}}}{\text{O}}}\limits_{\left[ {\text{D}} \right]} \)
The compound " A " is

1 1-Chloro propane
2 2-Chloro propane
3 Both of these
4 None of these
CHXI13:HYDROCARBONS

318068 The final solution left after kolbe's electrolysis in the manufacutre of ethene is

1 Alkaline
2 Acidic
3 Neutral
4 Cant be predicted.
CHXI13:HYDROCARBONS

318069 An alkyl chloride (A) produces a single alkene on reaction with sodium ethoxide and ethanol. The alkene further undergoes hydrogenation to yield 2-methylbutane. The alkyl chloride (A) is

1 \(\mathrm{ClCH}_{2} \mathrm{C}\left(\mathrm{CH}_{3}\right)_{3}\)
2 \(\mathrm{ClCH}_{2} \mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{CH}_{3}\)
3 \(\mathrm{ClCH}_{2} \mathrm{CH}\left(\mathrm{CH}_{3}\right) \mathrm{CH}_{2} \mathrm{CH}_{3}\)
4 \(\mathrm{CH}_{3} \mathrm{C}(\mathrm{Cl})\left(\mathrm{CH}_{3}\right) \mathrm{CH}_{2} \mathrm{CH}_{3}\)