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Mere Teacher · Previous Year Questions
JEE Main Chemistry · Amines · Set 10 (Q271-291)
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271.
In the following sequence of reactions; AReductionBHNO2CH3CH2OH
The compound A is
(1)propane nitrile
(2)ethane nitrile
(3)nitromethane
(4)methyl isocyanate.
272.
Hinsberg's reagent is
(1)C6H5SO2Cl
(2)C6H5SO2NH2
(3)CH3COCl/ pyridine
(4)(CH3CO)2O/ pyridine
273.
A secondary amine is
(1)compound with an NH2 group on the carbon atom in number 2 position
(2)a compound in which 2 of the hydrogen of NH3 have been replaced by organic groups
(3)an organic compound with two NH2 groups
(4)a compound with two carbon atoms and an NH2 group
274.
What are X and Y in the following reactions?
(X) (Y)
(1)CH3CH2OHH3PO2,H2O
(2)CH3MgXH3PO3
(3)Aliphatic diazonium salts liberate nitrogen gas quantitatively.
(4)Aniline cannot be converted into fluorobenzene via its diazonium salt
275.
In the given set of reactions: 2-Bromopropane →alc.AgCNheatX→LiAlH4YThe IUPAC name of product Y is
(1)N-isopropylmethanamine
(2)N-methylpropan-2-amine
(3)N-methylpropanamine
(4)butan-2-amine.
276.
Following is a confirmatory test for aromatic primary amines. Identify reagent (A) and (B). C6H5NH2(A)C6H5N2+Cl−(B)NaOH Scarlet red dye
(1)A=HNO3/H2SO4; B= phenol
(2)A=NaNO2+HCl,0-5∘C; B= aniline
(3)A=NaNO2+HCl,0-5∘C; B= 1-naphthol (α-naphthol)
(4)A=NaNO2+HCl,0-5∘C; B= 2-naphthol (β-naphthol)
277.
What is the IUPAC name of the below given compound?
(1)N - Methyl-N-ethylbenzenamine
(2)N - Methyl - N - phenylethanamine
(3)N-Ethyl- N - Methylbenzenamine
(4)N-Ethyl- N - phenylmethanamine
278.
R−CN(i) SnCl2+HCl(ii) H3O+R−CHO What is the name of the above reaction?
(1)Rosenmund
(2)Williamson
(3)Stephen
(4)Kolbe
279.
Given below are two statements : Statement I: Aniline reacts with con. H2SO4 followed by heating at 453−473K gives p- aminobenzene sulphonic acid, which gives blood red colour in the 'Lassaigne's test'. Statement II: In Friedel - Craft's alkylation and acylation reactions, aniline forms salt with the AlCl3 catalyst. Due to this, nitrogen of aniline aquires a positive charge and acts as deactivating group. In the light of the above statements, choose the correct answer from the options given below :
(1)Statement I is false but statement II is true
(2)Both statement I and statement II are false
(3)Statement I is true but statement II is false
(4)Both statement I and statement II are true
280.
A student performed analysis of 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−CH2−CH(NH2)−CH3
(2)(CH3)2CH−NH2
(3)CH3CH2CH2NH2
(4)Ph−CH(CH3)−NH2
281.
In the given reaction what is X?
(1)Isonitrile
(2)Nitrile
(3)Nitrite
(4)Oxime
282.
The final product R is
(1)
(2)
(3)
(4)
283.
The structure of X is:
(1)
(2)
(3)
(4)
284.
C2H5BrexcessNH3ABr2KOHB What is B in the given reaction?
(1)
(2)
(3)
(4)
285.
An organic compound 'A' contains nitrogen and chlorine. It dissolves readily in water to give a solution that turns litmus red. Titration of compound 'A' with standard base indicates that the molecular weight of 'A5 is 131 ± 2. When a sample of £A' is treated with aq. NaOH, a liquid separates which contains N but not Cl. Treatment of the obtained liquid with nitrous acid followed by phenol gives orange precipitate. The compound 'A' is :
(1)
(2)
(3)
(4)
286.
What is IUPAC name of allylamine?
(1)Propan-1-amine
(2)Prop-2-en-1-amine
(3)Prop-1-en-2amine
(4)Propan-2-amine
287.
Indentify X in the following.
(1)
(2)
(3)
(4)
288.
CH3-CH2-CNCH3MgBrEtherAH3O+BZn-HgHClC The correct structure of C is
(1)CH3-CH2-CH2-CH3
(2)CH3−CH2−C(=O)−CH3
(3)CH3−CH2−CH(OH)−CH3
(4)CH3—CH2—CH = CH2
289.
Identify the product formed (A and E)
(1)
(2)
(3)
(4)
290.
P1. CH3MgBr2. H3O+R1. dil. NaOH2. Δ 4-methylpent-3-en-2-one P is