Reactions of Alkyl Halides
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Q. The compound which undergoes SN1 reaction most rapidly is:
Q.
Name a gas which gives a black ppt when passed through copper sulphate solution.
Q. Which of the following compound will undergo SN1 reaction?
- All the above
Q. An optically active compound A upon acid catalysed hydrolysis yields two optically active compounds B and C by pseudo first order kinetics with respect to A. The observed rotation of the mixture after 20 min was 5° while after completion of the reaction it was – 20°. If optical rotation per molar concentration of A, B and C are 60°, 40° and – 80° respectively and observed rotation of a compound is directly proportional to concentration of that compound. (Take optical rotation in degree)
List -IList -II(I) Rate constant of the reaction (in hour−1)(P)1.0(II) Initial concentration of compound A (in M)(Q)2.08(III) If the initial concentratrion of A is 0.8 M then(R)0.5the observed optical rotation of mixture after 1 hour(IV) If initially along with A;B and C are also present with(S)−22initial concentration [A] = 0.4M, [B] = 0.1 M and [C] = 0.2 Mthen net observed optical rotation of the mixture after 40 min.(T)22(U)−18
Which of the following options has the correct combination considering List-I and List-II
List -IList -II(I) Rate constant of the reaction (in hour−1)(P)1.0(II) Initial concentration of compound A (in M)(Q)2.08(III) If the initial concentratrion of A is 0.8 M then(R)0.5the observed optical rotation of mixture after 1 hour(IV) If initially along with A;B and C are also present with(S)−22initial concentration [A] = 0.4M, [B] = 0.1 M and [C] = 0.2 Mthen net observed optical rotation of the mixture after 40 min.(T)22(U)−18
Which of the following options has the correct combination considering List-I and List-II
- (III), (U)
- (IV), (U)
- (III), (S)
- (IV), (S)
Q. During the course of a SN1 reaction, the intermediate species formed is:
- a carbocation
- a free radical
- an intermediate complex
- a carbanion
Q. The decreasing order of relative nucleophilicity of the following nucleophiles in a protic solvent is
SH−, AcO−, PhO−, OH−, H2O
SH−, AcO−, PhO−, OH−, H2O
- SH−>OH−>H2O>AcO−>PhO−
- SH−>OH−>PhO−>AcO−>H2O
- SH−>PhO−>OH−>H2O>AcO−
- OH−>SH−>PhO−>AcO−>H2O
Q. In a Nucleophilic substitution unimolecular (SN1) reaction:
- Formation of carbocation intermediate takes place.
- Formation of carbanion intermediate takes place.
- None of the above.
- Formation of free radical intermediate takes place.
Q. The order of decreasing nucleophilicity is
- H2O>OH−>CH3COO−>CH3O−
- CH3COO−>CH3O−>HO−>H2O
- HO−>CH3O−>CH3COO−>H2O
- CH3O−>OH−>CH3COO−>H2O