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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
In the following pair of halogen compounds, which compound undergoes a faster SN1 reaction?
Write the structure of the major organic product in the following reaction:
\[\ce{CH3CH(Br)CH2CH3 + NaOH ->[water]}\]
Write the mechanism of the following reaction:
\[\ce{{n}BuBr + KCN ->[EtOH-H2O] {n}BuCN}\]
What happens when chlorobenzene is subjected to hydrolysis?
AgCN reacts with haloalkanes to form isocyanide. Haloalkanes react with KCN to form alkyl cyanides as the main product. Why?
In the reaction, \[\ce{R - X + NaOR' -> ROR’ + X}\] ( – ve ion). The main product formed is:
Which one is most reactive towards SN1 reaction?
The order of reactivities of the following alkyl halides for an SN2 reaction is:
The process of separation of a racemic modification into d and l-enantiomers is called ____________.
Which of the following is a chiral compound?
SN1 reaction of alkyl halides lead to ___________.
The increasing order of nucleophilicity would be:
The correct order of increasing the reactivity of C–X bond towards nucleophile in following compounds.
(I)
(II)
(CH3)3CCl
(III)
(CH3)2CHCl
(IV)
Assertion: KCN reacts with methyl chloride to give methyl isocyanide.
Reason: CN– is an ambident nucleophile.
Which of the following statements are correct about this reaction?
(i) The given reaction follows SN2 mechanism.
(ii) (b) and (d) have opposite configuration.
(iii) (b) and (d) have same configuration.
(iv) The given reaction follows SN1 mechanism.
The number of chiral carbons present in the molecule given below is ______.
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2-Bromopentane, 1-Bromopentane, 2-Bromo-2-methylbutane
Which alkyl halide from the following pair would you expect to react more rapidly by an SN2 mechanism? Explain your answer.
\[\begin{array}{cc}\ce{CH3CH2CHCH3}\\\phantom{...}|\\\phantom{....}\ce{Br}\end{array}\] or \[\begin{array}{cc}\phantom{.....}\ce{CH3}\\\phantom{..}|\\\ce{H3C - C - Br}\\\phantom{..}|\\\phantom{....}\ce{CH3}\end{array}\]
