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19,000+ solved questions for JEE Advanced, JEE Mains, NEET & IChO — with answers and expert explanations.

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MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryAlkyl and Aryl Halides

In alkaline hydrolysis of a tertiary halide by aqueous solution of alkali if concentration of alkali is doubled, then the reaction (AIIMS 2012)

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryAlkyl and Aryl Halides

In the following sequence of reaction, H O LiAlH KCN CH Br A B C, -> -> -> C is (CBSE AIPMT 2012)

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryAlkyl and Aryl Halides

In the replacement reaction The reaction will be most favourable if M happens to be (AIPMT 2012)

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryAlkyl and Aryl Halides

KOH alcohol CH CH CH Br CH CH CH -> The above reaction is an example of …… reaction. (OJEE 2011)

MEDIUMMCQ SINGLENEET 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 SINGLENEET 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 SINGLENEET 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 SINGLENEET 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 SINGLENEET ChemistryInorganic ChemistryAlkyl and Aryl Halides

Which of the following alkyl halides is hydrolysed by SN2 mechanism? (BVP 2011) (a) C H CH Br (b) CH Br (c) CH CHCH Br

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryAlkyl and Aryl Halides

Following is the substitution reaction in which –CN replaced –Cl (Alcoholic) R Cl KCN R CN KCl -> To obtain propanenitrile, R-Cl should be (KCET 2011)

MEDIUMMCQ SINGLENEET 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 SINGLENEET ChemistryInorganic ChemistryAlkyl and Aryl Halides

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

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryAlkyl and Aryl Halides

Which one of the following is not true for the hydrolysis of t-butyl bromide with aqueous NaOH? (KCET 2011)

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryAlkyl and Aryl Halides

Given reaction, ‘Y’ in the reaction is (DUMET 2011)

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryAlkyl and Aryl Halides

Consider the reactions. (i) C H OH CH CH CH Br CH CH CH OC H HBr -> (ii) C H O CH CH CH Br CH CH CH OC H HBr -> The mechanisms of reactions (i) and (ii) are respectively …

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryAlkyl and Aryl Halides

Which one is most reactive towards SN1 reaction? (AIPMT 2011)

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryAlkyl and Aryl Halides

Identify Z, in the following series. Br alc.KOH KCN C H I X Y Z -> -> -> (VMMC 2010) (a) CH CH CN (b) NCCH CH CN (c) BrCH CH CN

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryAlkyl and Aryl Halides

The reactivities of CH Cl,CH CH CH Cl and C H Cl are in the order (CMC 2010) (a) CH Cl CH CH Cl C H Cl (b) CH CH CH Cl CH Cl C H Cl (c) C H Cl CH CH CH Cl CH Cl (d) CH Cl C H Cl CH CH C…

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryAlkyl and Aryl Halides

Haloforms are trihalogen derivatives of

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryAlkyl and Aryl Halides

Θ H C-SNa +CH CH -X -> The reaction is fastest when X is:

MEDIUMMCQ SINGLENEET 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 SINGLENEET ChemistryInorganic ChemistryAlkyl and Aryl Halides

KSH -> P should be (a) (b)

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryAlkyl and Aryl Halides

Major (Excess) CH CH NH CH I P -> P should be

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryAlkyl and Aryl Halides

Among the following alkyl halides, choose the one with the lowest boiling point.

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryAlkyl and Aryl Halides

Which of the following has the highest normal boiling point?

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