Advertisements
Advertisements
प्रश्न
Complete the reaction with the main product formed:

Advertisements
उत्तर

APPEARS IN
संबंधित प्रश्न
Write the main products when methyl chloride is treated with AgCN.
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:
\[\ce{{n}BuBr + KCN ->[EtOH-H2O] {n}BuCN}\]
Arrange the compounds of the following set in order of reactivity towards SN2 displacement:
1-Bromobutane, 1-Bromo-2, 2-dimethylpropane, 1-Bromo-2-methylbutane, 1-Bromo-3-methylbutane
SN2 mechanism proceeds through intervention of ____________.
Identify the end product (C) in the following sequence:
\[\ce{C2H5OH ->[SOCl2][Pyridine] A ->[KCN {(alc.)}] B ->[2H2O/H^+] C}\]
The correct order of increasing the reactivity of C–X bond towards nucleophile in following compounds.

(I)

(II)
(CH3)3CCl
(III)
(CH3)2CHCl
(IV)
The increasing order of reactivity towards SN1 mechanism is:
(I) \[\begin{array}{cc}
\ce{CH3-CH-CH2-CH3}\\
|\phantom{........}\\
\ce{CH3}\phantom{.....}
\end{array}\]
(II) CH3CH2CH2Cl
(III) P–CH3O–C6H4–CH2Cl
Which reagent will you use for the following reaction?
\[\ce{CH3CH2CH2CH3 -> CH3CH2CH2CH2Cl + CH3CH2CHClCH3}\]

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.
