‘A’ and ‘B’ formed in the following set of reactions are: [2023]
[IMAGE 208]
[IMAGE 209]
[IMAGE 210]
[IMAGE 211]
[IMAGE 212]
(4)
[IMAGE 213]
Compound A, , given a tetraacetate with and oxidation of A with gives an acid, . Reduction of A with HI gives isopentane. The possible structure of A is: [2023]
[IMAGE 214]
[IMAGE 215]
[IMAGE 216]
[IMAGE 217]
(3)
[IMAGE 218]
Decreasing order of dehydration of the following alcohols is [2023]
[IMAGE 219]
a > d > b > c
d > b > c > a
b > a > d > c
b > d > c > a
(4)
Ease of dehydration stability of carbocation.
A solution of in amyl alcohol has a ______ colour. [2023]
Yellow
Orange-Red
Green
Blue
(4)
is more soluble in organic solvent like amyl alcohol and blue coloured organic layer is obtained.
In the following reaction, ‘B’ is [2023]
[IMAGE 220]
[IMAGE 221]
[IMAGE 222]
[IMAGE 223]
[IMAGE 224]
(4)
[IMAGE 225]
The strongest acid from the following is [2023]
[IMAGE 226]
[IMAGE 227]
[IMAGE 228]
[IMAGE 229]
(1)
Due to presence of — group at meta position, phenoxide ion formed is the most stabilised conjugate ion, therefore, its corresponding compound is the strongest acid. Hence the compound [IMAGE 230] is the strongest acid among the given.
Given below are two statements: One is labelled as Assertion A and the other is labelled as Reason R.
Assertion A: Butan-1-ol has higher boiling point than ethoxyethane.
Reason R: Extensive hydrogen bonding leads to stronger association of molecules.
In the light of the above statements, choose the correct answer from the options given below: [2023]
Both A and R are true but R is not the correct explanation of A
A is false but R is true
Both A and R are true and R is the correct explanation of A
A is true but R is false
(3)
Due to intermolecular hydrogen bonding in Butane-1-ol, association of molecule increases resulting increase in attraction between the molecules and hence boiling point increases.
Incorrect method of preparation for alcohols from the following is: [2023]
Reaction of ketone with RMgBr followed by hydrolysis
Reaction of alkyl halide with aqueous NaOH.
Ozonolysis of alkene.
Hydroboration–oxidation of alkene.
(3)
In ozonolysis of alkene aldehydes or ketones are formed as product.
[IMAGE 231]
[IMAGE 232]
Product [X] formed in the above reaction is: [2023]
[IMAGE 233]
[IMAGE 234]
(2)
[IMAGE 235]
In the reaction given below:
[IMAGE 236]
'B' is: [2023]
[IMAGE 237]
[IMAGE 238]
[IMAGE 239]
[IMAGE 240]
(3)
[IMAGE 241]