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MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryAlkyl and Aryl Halides

Assertion: Consider the following SN2 reactions. (I) and (II) Reaction (II) occurs at a faster rate than (I) Reason: Anion of reaction (II) is a stronger base than the anion of reaction (I).

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryAlkyl and Aryl Halides

Assertion: Allyl halide (CH2=CH–CH2X) is more reactive than CH3CH2CH2X in a SN2 reaction. Reason: Allyl halide forms a resonance stabilized carbocation

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryAlkyl and Aryl Halides

Assertion: SN2 reaction of CH3––Br is faster in Cl CH S – SCH3 Cl (CH ) CHS 3 2 – SCH(CH ) 3 2 DMSO than in H2O. Reason: DMSO has greater capability to solvate nucleophile.

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryAlkyl and Aryl Halides

Assertion: Chlorination of allylic hydrogen is difficult than vinylic hydrogen. Reason: Allyl radical is stabilised by resonance.

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryAlkyl and Aryl Halides

Assertion: Treatment of either enantiomer of 2-chlorobutane with ethanolic KOH results in trans-2- butene as major elimination product. Reason: Elimination with ethanolic KOH is a bimolecular reaction.

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryAlkyl and Aryl Halides

Assertion: Ph–CO–CH2CH2OCH3 has greater reactivity for E1CB than for E2 reaction. Reason: A poor leaving group and acidic —H favour E1CB mechanism.

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryAlkyl and Aryl Halides

Assertion: The reaction of bulky base such as potassium tertiary butoxide [(CH3)3CO–K+] with secondary alkyl halides gives predominantly E2 elimination product rather than SN2 substitution product. Reason: The transit…

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryAlkyl and Aryl Halides

Assertion: p-nitrochlorobenzene is more reactive than m-nitrochlorobenzene towards aromatic nucleophilic substitution reaction. Reason: Nitro group from para and meta positions has opposite effect in aromatic nucleoph…

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryAlkyl and Aryl Halides

Assertion: A dichlorobenzene is slightly more reactive than chlorobenzene towards an aromatic nucleophilic substitution reaction. Reason: Chlorine has electron withdrawing effect on aromatic ring.

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryAlkyl and Aryl Halides

Assertion: Chloral reacts with phenyl chloride to form DDT. Reason: It is an electrophilic substitution reaction

MEDIUMMCQ SINGLEJEE Advanced ChemistryOrganic ChemistryAldehydes and ketones

The IUPAC name of Cl3CCH2CHO is :

MEDIUMMCQ SINGLEJEE Advanced ChemistryOrganic ChemistryAldehydes and ketones

Conc.NaOH O|| H C H CH CH O -> Find out the products of reaction (AIIMS 2019)

MEDIUMMCQ SINGLEJEE Advanced ChemistryOrganic ChemistryAldehydes and ketones

Product in following reaction is CH3MgI + HCHO → Product

MEDIUMMCQ SINGLEJEE Advanced ChemistryOrganic ChemistryAldehydes and ketones

Grignard reagent on reaction with acetone forms

MEDIUMMCQ SINGLEJEE Advanced ChemistryOrganic ChemistryAldehydes and ketones

Which of the following species is the conjugate acid of the hemiacetal formed by reaction of benzaldehyde with methanol containing a trace of acid ? (a) (b) (c) (d)

MEDIUMMCQ SINGLEJEE Advanced ChemistryOrganic ChemistryAldehydes and ketones

Benzaldehyde condenses with N,N-dimethylaniline in presence of anhydrous ZnCl2 to give

MEDIUMMCQ SINGLEJEE Advanced ChemistryOrganic ChemistryAldehydes and ketones

Which one of the following does not form sodium bisulphite addition product with sodium bisulphite solution

MEDIUMMCQ SINGLEJEE Advanced ChemistryOrganic ChemistryAldehydes and ketones

Reaction of acetaldehyde with HCN followed by hydrolysis gives a compound which shows

MEDIUMMCQ SINGLEJEE Advanced ChemistryOrganic ChemistryAldehydes and ketones

A and B in the following reactions are (a) (b) (c)

MEDIUMMCQ SINGLEJEE Advanced ChemistryOrganic ChemistryAldehydes and ketones

The most reactive compound towards formation of cyanohydrin on treatment with HCN followed by acidification is

MEDIUMMCQ SINGLEJEE Advanced ChemistryOrganic ChemistryAldehydes and ketones

Correct order of reactivity of CH3CHO, C2H5COCH3 and CH3COCH3 is

MEDIUMMCQ SINGLEJEE Advanced ChemistryOrganic ChemistryAldehydes and ketones

Which of the following carbonyl oxygen will form strongest hydrogen bond with 퐻2푂 molecule? (a) (b) (c) (d)

MEDIUMMCQ SINGLEJEE Advanced ChemistryOrganic ChemistryAldehydes and ketones

Product may be

MEDIUMMCQ SINGLEJEE Advanced ChemistryOrganic ChemistryAldehydes and ketones

Which of the aldehyde is most reactive towards nucleophilic addition reaction ?

MEDIUMMCQ SINGLEJEE Advanced ChemistryOrganic ChemistryAldehydes and ketones

Nucleophilic addition reaction will be most favoured in

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