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Amines

JEE Main 2026 (Online) 2nd April Evening ShiftNumericalMedium📈 Topic in 39% papers+4
Ques. 1JEE Main 2026, 2 April (Evening Shift)

Consider the following reactions sequence [figure] When the product (P) is subjected to Carius analysis using AgNO3, 1.0 g of the product (P) will produce g of the precipitate of AgBr. (Nearest Integer) (Given : molar mass in g mol-1 C : 12, H : 1, O : 16, N : 14, Br : 80, Ag : 108)

Answer

1

Solution

(i) Sn/HCl, then OH : –NO2 → –NH2 (p-toluidine)

(ii) (CH3CO)2O: –NH2 → –NHCOCH3 (activation is moderated, monosubstitution)

(iii) Br2/AlBr3: para position is blocked by –CH3; –NHCOCH3 is the stronger o/p director ⇒ Br enters ortho to –NHCOCH3

(iv) H3O : amide hydrolysed back to –NH2

⇒ P = 2-bromo-4-methylaniline [figure] , C7H8BrN

M(P) = 84 + 8 + 80 + 14 = 186 g mol-1; M(AgBr) = 188 g mol-1

1 mol P (1 Br) → 1 mol AgBr ⇒ mass of AgBr = 1.0186 188 = 1.01 g ≈ 1 g

Answer: 1

Keep practising — Amines

Ques. 2JEE Main 2026, 28 January (Morning Shift)

Consider the following reactions giving major product. Identify the correct reaction.

  1. [figure]
  2. [figure]
  3. [figure]
  4. H3CCH2- O \|C-NH2 + Br2 + 4 KOH (alc) H3CCH2NH2 + 2KBr + K2CO3 + 2H2O
Ques. 3JEE Main 2026, 28 January (Evening Shift)

A student performed analysis of an aliphatic organic compound 'X' which on analysis gave C = 61.01%, H = 15.25%, N = 23.74%. This compound, on treatment with HNO2/H2O, produced another compound 'Y' which did not contain any nitrogen atom. However, the compound 'Y' upon controlled oxidation produced another compound 'Z' that responded to iodoform test. The structure of 'X' is :

  1. CH3-CH2CH(NH2)-CH3
  2. CH3CH2CH2NH2
  3. Ph-CH(CH3)-NH2
  4. [figure]
Ques. 4JEE Main 2026, 28 January (Evening Shift)

Total number of alkali-insoluble solid sulphonamides obtained by reaction of given amines with Hinsberg's reagent is . Aniline, N-Methylaniline, Methanamine, N,N-Dimethylmethanamine, N-Methylmethanamine, Phenylmethanamine, N-Propylaniline, N-Phenylaniline, N,N-Dimethylaniline, Allylamine, Isopropylamine

  1. 8
  2. 5
  3. 2
  4. 4
Ques. 5JEE Main 2026, 24 January (Morning Shift)

The correct stability order of the following diazonium salts is [figure]

  1. C > D > B > A
  2. A > C > D > B
  3. A > B > C > D
  4. C > A > D > B
Ques. 6JEE Main 2026, 24 January (Evening Shift)

Given below are two statements : In the light of the above statements, choose the correct answer from the options given below

  1. Both Statement I and Statement II are false
  2. Statement I is false but Statement II is true
  3. Statement I is true but Statement II is false
  4. Both Statement I and Statement II are true
Ques. 7JEE Main 2026, 23 January (Morning Shift)

Consider the following sequence of reactions. [figure] Assuming that the reaction proceeds to completion, then 137 mg of 4-nitrotoluene will produce mg of B. (Given molar mass in g mol-1 H : 1, C : 12, N : 14, O : 16, Br : 80)

  1. 208
  2. 228
  3. 146
  4. 301
Ques. 8JEE Main 2026, 23 January (Morning Shift)

Compound 'P' undergoes the following sequence of reactions : [figure] 'P' is :

  1. [figure]
  2. [figure]
  3. [figure]
  4. [figure]
Ques. 9JEE Main 2026, 23 January (Evening Shift)

Given below are two statements : In the light of the above statements, choose the correct answer from the options given below

  1. Both Statement I and Statement II are true
  2. Statement I is false but Statement II is true
  3. Statement I is true but Statement II is false
  4. Both Statement I and Statement II are false
Ques. 10JEE Main 2026, 23 January (Evening Shift)

A student has been given a compound 'x' of molecular formula C6H7N. 'x' is sparingly soluble in water. However, on addition of dilute mineral acid, 'x' becomes soluble in water. 'x' when treated with CHCl3 and KOH(alc), 'y' is produced. 'y' has a specific unpleasant smell. On treatment with benzenesulphonyl chloride, 'x' gives a compound 'z' which is soluble in alkali. The number of different "H" atoms present in 'z' is :

  1. 8
  2. 4
  3. 5
  4. 7
Ques. 11JEE Main 2026, 22 January (Morning Shift)

'A' is a neutral organic compound (M.F. : C8H9ON). On treatment with aqueous Br2/HO , 'A' forms a compound 'B' which is soluble in dilute acid. 'B' on treatment with aqueous NaNO2/HCl (0-5 C) produces a compound 'C' which on treatment with CuCN/NaCN produces 'D'. Hydrolysis of 'D' produces 'E' which is also obtainable from the hydrolysis of 'A'. 'E' on treatment with acidified KMnO4 produces 'F'. 'F' contains two different types of hydrogen atoms. The structure of 'A' is

  1. [figure]
  2. [figure]
  3. [figure]
  4. [figure]

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