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प्रश्न
Write the structure of the major organic product in the following reaction:
\[\ce{CH3CH2CH2OH + SOCl2 ->}\]
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उत्तर
\[\ce{\underset{Propan-1-ol}{CH3CH2CH2OH} + SOCl2 ->[nucleophilic substitution] \underset{1-Chloropropane}{CH3CH2CH2Cl} + HCl\uparrow + SO2\uparrow}\]
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संबंधित प्रश्न
Which would undergo SN2 reaction faster in the following pair and why ?

Write the structure of the major product in each of the following reaction :

The treatment of alkyl chlorides with aqueous KOH leads to the formation of alcohols but in the presence of alcoholic KOH, alkenes are major products. Explain.
What is the action of the following on ethyl bromide?
silver acetate
AgCN reacts with haloalkanes to form isocyanide. Haloalkanes react with KCN to form alkyl cyanides as the main product. Why?
Arrange the following organic compounds in descending order of their reactivity towards SN1 reaction.
C6H5CH2Br, C6H5CH(C6H5)Br, C6H5CH(CH3)Br, C6H5C(CH3)(C6H5)Br
2-Bromopentane is heated with potassium ethoxide in ethanol. The major product obtained is ____________.
Which reagent will you use for the following reaction?
\[\ce{CH3CH2CH2CH3 -> CH3CH2CH2CH2Cl + CH3CH2CHClCH3}\]
A primary alkyl halide would prefer to undergo ______.

Which of the statements are correct about above reaction?
(i) (a) and (e) both are nucleophiles.
(ii) In (c) carbon atom is sp3 hybridised.
(iii) In (c) carbon atom is sp2 hybridised.
(iv) (a) and (e) both are electrophiles.
How do polar solvents help in the first step in SN1 mechanism?
Which of the following is the definition of chirality?
CCl4 is insoluble in water because:-
Which one of the following compounds is more reactive towards SN1 reaction?
In SN1 reactions, the correct order of reactivity for the following compounds:
CH3Cl, CH3CH2Cl, (CH3)2CHCl and (CH3)3CCl is ______.
Arrange the following compounds in increasing order of reactivity towards SN2 reaction.
2-Bromopentane, 1-Bromopentane, 2-Bromo-2-methylbutane
Inversion of configuration occurs in ______.
Consider the reactions,
(i) \[\begin{array}{cc}
\phantom{}\ce{\underset{}{(CH3)2CH - CH2Br} ->[C2H5OH] \underset{}{(CH3)2CH - CH2OC2H5 + HBr}}\\
\end{array}\]
(ii) \[\begin{array}{cc}
\phantom{}\ce{\underset{}{(CH3)2CH - CH2Br} ->[C2H5O-] \underset{}{(CH3)2CH - CH2OC2H5 + Br-}}\\
\end{array}\]
The mechanisms of reactions (i) and (ii) are respectively:
Which of the following reactions is an example of nucleophilic substitution reaction?
