12th Chemistry Sura Guide

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    12th Chemistry Sura Guide. We covered all the 12th Chemistry Sura Guide MCQs in this post for free so that you can practice well for the exam.

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    12th Chemistry Sura Guide Objective for Students

    Quick Quiz

    Sodium phenate reacts with acetyl chloride to form:

    (A) Methyl benzoate

    (B) Acetyl phenol

    (C) Phenylacetate

    (D) Chlorobenzene

    Option c – Phenylacetate

    Which of the following is not a phenolic compound ( 12th Chemistry Sura Guide MCQ )

    (A) Salol

    (B) o-Cresol

    (C) Anisole

    (D) Quinol

    Option c – Anisole

    An unacceptable name for a compound containing one -OH group attached to the benzene nucleus would be:

    (A) Carbolic acid

    (B) Hydroxybenzene

    (C) Catechol

    (D) Phenol

    Option c – Catechol

    Isopropyl alcohol on oxidation gives ( 12th Chemistry Sura Guide MCQ )

    (A) Acetone

    (B) Acetaldehyde

    (C) Ether

    (D) Ethylene

    Option a – Acetone

    The highest boiling point is of:

    (A) Ethanol

    (B) Ether

    (C) Alkane

    (D) Aldehyde

    Option a – Ethanol

    In the reaction of glucose → ethyl alcohol, the enzyme involved is ( 12th Chemistry Sura Guide MCQ )

    (A) Zymase

    (B) Invertase

    (C) Maltase

    (D) Diastase

    Option a – Zymase

    Which compound has the highest boiling point?

    (A) Acetone

    (B) Diethyl ether

    (C) Methanol

    (D) Ethanol

    Option d – Ethanol

    Reimer-Tiemann reaction involves ( 12th Chemistry Sura Guide MCQ )

    (A) Carbanion intermediate

    (B) A carbene intermediate

    (C) Carbonium ion intermediate

    (D) Free radical intermediate

    Option b – A carbene intermediate

    Phenol with Hinsberg’s reagent gives:

    (A) Sulphone

    (B) Sulphanilic acid

    (C) Sulphonic ester

    (D) Sulphonal

    Option c – Sulphonic ester

    Electrophilic substitution reactions in phenol take place at ( 12th Chemistry Sura Guide MCQ )

    (A) p-position

    (B) m-position

    (C) o-position

    (D) o- and p-positions

    Option d – o- and p-positions

    Condensation of phenol and phthalic anhydride gives:

    (A) Methyl orange

    (B) Phenol red

    (C) Salicylic acid

    (D) Phenolphthalein

    Option d – Phenolphthalein

    The major product obtained from the interaction of phenol with sodium hydroxide and carbon dioxide is ( 12th Chemistry Sura Guide MCQ )

    (A) Salicylaldehyde

    (B) Salicylic acid

    (C) Phthalic acid

    (D) Benzoic acid

    Option b – Salicylic acid

    Phenyl magnesium bromide on reacting with ethanol forms:

    (A) Phenol

    (B) Benzene

    (C) Ethane

    (D) Isopropyl phenyl ether

    Option b – Benzene

    In Williamson’s synthesis, ethoxyethane is prepared by ( 12th Chemistry Sura Guide MCQ )

    (A) Passing ethanol over heated alumina

    (B) Sodium ethoxide with ethyl bromide

    (C) Ethyl alcohol with sulfuric acid

    (D) Ethyl iodide and dry silver oxide

    Option b – Sodium ethoxide with ethyl bromide

    Ethyl chloride is converted into diethyl ether by:

    (A) Wurtz synthesis

    (B) Grignard reaction

    (C) Perkin’s reaction

    (D) Williamson’s synthesis

    Option d – Williamson’s synthesis

    In Williamson’s synthesis for diethyl ether, which species works as a nucleophile ( 12th Chemistry Sura Guide MCQ )

    (A) Halide ion

    (B) Ethoxide ion

    (C) Ethyde ion

    (D) Hydride ion

    Option b – Ethoxide ion

    The preparation of ethers from alcohols by using sulfuric acid is called:

    (A) Williamson’s ether synthesis

    (B) Williamson’s continuous etherification process

    (C) Ziesel’s method

    (D) Zerewitinoff method

    Option b – Williamson’s continuous etherification process

    The reaction of ethyl iodide with sodium ethoxide is ( 12th Chemistry Sura Guide MCQ )

    (A) An electrophilic substitution reaction

    (B) A nucleophilic addition reaction

    (C) A nucleophilic substitution reaction

    (D) A free radical substitution reaction

    Option c – A nucleophilic substitution reaction

    The first member of the ether series on reaction with sodium and liquified ammonia gives:

    (A) Methanol + methane

    (B) Ethane + methanol

    (C) Ethanol

    (D) Ethane

    Option a – Methanol + methane

    Mark the correct statement ( 12th Chemistry Sura Guide MCQ )

    (A) Ethers behave as Lewis base

    (B) Ethers form coordination complexes with Lewis acids

    (C) With cold HI diethyl ether gives ethyl alcohol & ethyl iodide

    (D) All are correct

    Option d – All are correct

    Ether on carbonylation gives:

    (A) Alkanoic acid

    (B) Alkanone

    (C) Alkyl alkanoate

    (D) Alkanal

    Option c – Alkyl alkanoate

    Diethyl ether absorbs oxygen to form ( 12th Chemistry Sura Guide MCQ )

    (A) Red-colored sweet-smelling compound

    (B) Acetic acid

    (C) Ether suboxide

    (D) Ether peroxide

    Option d – Ether peroxide

    Diethyl ether and air give ether-hydroperoxide. The mechanism of the reaction is:

    (A) Nucleophilic substitution

    (B) Free radical addition

    (C) Free radical substitution

    (D) None of the above

    Option b – Free radical addition

    The order of reactivity of halogen acids with ether is ( 12th Chemistry Sura Guide MCQ )

    (A) HCl > HBr > HI

    (B) HI > HBr > HCl

    (C) HCl > HI > HBr

    (D) HI > HCl > HBr

    Option b – HI > HBr > HCl

    Isopropyl n-propyl ether is obtained by reacting 1-bromopropane with:

    (A) Sodium ‘n-propoxide

    (B) Sodium ethoxide

    (C) Sodium isopropoxide

    (D) Sodium bromide

    Option c – Sodium isopropoxide

    Ethyl acetate is prepared from ( 12th Chemistry Sura Guide MCQ )

    (A) Silver methanoate and methyl alcohol

    (B) Silver ethanoate and ethyl alcohol

    (C) Silver methanoate and ethanol

    (D) Silver ethanoate and ethyl bromide

    Option d – Silver ethanoate and ethyl bromide

    During the dehydrohalogenation of haloalkanes, the formation of the major product is decided on the basis of:

    (A) Popff’s rule

    (B) Saytzeff’s rule

    (C) Peroxide rule

    (D) Markonikoff’s rule

    Option b – Saytzeff’s rule

    Elimination of HI from 2-iodo-2-methylbutane forms ( 12th Chemistry Sura Guide MCQ )

    (A) 2-Methylbut-2-ene

    (B) 2-Methylbut-1-ene

    (C) 3-Methylbut-1-ene

    (D) Isopentyl alcohol

    Option a – 2-Methylbut-2-ene

    Organometallic compounds must have:

    (A) Carbon-Oxygen bond

    (B) Carbon-Metal bond

    (C) Metal-Halogen bond

    (D) Non-Metal atom

    Option b – Carbon-Metal bond

    Isopropyl iodide, on heating with excess alcoholic ammonia, produces:

    (A) Trimethylamine

    (B) Diethylamine

    (C) Propan-1-amine

    (D) Propan-2-amine

    Option d – Propan-2-amine

    1-Bromopropane, on boiling with alcoholic potassium nitrite, gives:

    (A) 1-Nitropropane

    (B) 2-Nitropropanate

    (C) n-Propyl nitrite

    (D) Sec-propyl nitrite

    Option c – n-Propyl nitrite

    During the alkaline hydrolysis of d-3-chloro-3-methylhexane, the product formed is:

    (A) Levo rotatory

    (B) Dextro rotatory

    (C) No rotation

    (D) Optically inactive

    Option d – Optically inactive

    Benzene, on reacting with bromine in the presence of Fe, produces:

    (A) Benzyl bromide

    (B) Bromobenzene

    (C) o-Bromobenzene

    (D) m-Bromobenzene

    Option b – Bromobenzene

    When chlorobenzene reacts with acetyl chloride, it gives:

    (A) p-Chloroacetophenone

    (B) Chloroacetobenzene

    (C) Acetophenyl chloride

    (D) Methyl aceto chlorobenzene

    Option a – p-Chloroacetophenone

    The transition state is defined as the state of a reaction, which contains:

    (A) Potential energy

    (B) Maximum energy

    (C) Zero energy

    (D) Minimum energy

    Option b – Maximum energy

    The oxidation product of trichloromethane is:

    (A) Phosgene

    (B) Sulphonyl chloride

    (C) Ethane

    (D) Dichloromethane

    Option a – Phosgene

    Which of the following can damage the cornea on direct contact?

    (A) Trichloromethane

    (B) Dichloromethane

    (C) Tetrachloromethane

    (D) Dichlorodifluoromethane

    Option b – Dichloromethane

    The reaction between haloalkane and haloarenes to give alkylbenzene in the presence of sodium metal is:

    (A) Groove’s reaction

    (B) Wurtz reaction

    (C) Fittig’s reaction

    (D) Wurtz-Fittig reaction

    Option d – Wurtz-Fittig reaction

    The temperature required to convert 1-chloro-4-nitrobenzene into 4-nitrophenol is:

    (A) 433K

    (B) 623K

    (C) 443K

    (D) 523K

    Option a – 433K

    Which of the following groups increases the rate of alkaline hydrolysis of haloarenes?

    (A) Nitro group

    (B) Alkyl radical

    (C) Electron-donating

    (D) Electron-repelling

    Option a – Nitro group

    Electrophilic substitution in phenyl chloride is possible due to:

    (A) Positive inductive effect of the halogen atom

    (B) Negative inductive effect of the halogen atom

    (C) Positive resonance effect of the halogen atom

    (D) Negative resonance effect of the halogen atom

    Option c – Positive resonance effect of the halogen atom

    Major chlorination product of chlorobenzene is:

    (A) 1,2-dichlorobenzene

    (B) p-dichlorobenzene

    (C) 1,3-dichlorobenzene

    (D) o-dichlorobenzene

    Option b – p-dichlorobenzene

    Conversion of benzene into phenyl bromide is:

    (A) Electrophilic addition reaction

    (B) Electrophilic substitution reaction

    (C) Nucleophilic addition reaction

    (D) Nucleophilic substitution reaction

    Option b – Electrophilic substitution reaction

    Phenyl amine reacts with sodium nitrite and dil. hydrochloric acid produces:

    (A) Chlorobenzene

    (B) Benzene diazonium chloride

    (C) Phenyl ammonium chloride

    (D) Benzyl chloride

    Option b – Benzene diazonium chloride

    Geminal and vicinal dihalides are:

    (A) Chain isomerism

    (B) Position isomerism

    (C) Electrophilic addition

    (D) Nucleophilic addition

    Option b – Position isomerism

    For the preparation of propane nitrile from bromoethane, the other reactant is:

    (A) HCN

    (B) HNC

    (C) KCN

    (D) AgCN

    Option c – KCN

    Chlorination of methane is:

    (A) Electrophilic substitution

    (B) Nucleophilic substitution

    (C) Free radical substitution

    (D) Nucleophilic addition

    Option c – Free radical substitution

    Major acylation product of chlorobenzene is:

    (A) 4-Chloro acetophenone

    (B) 3-Chloro acetophenone

    (C) 2-Chloro acetophenone

    (D) m-Chloro acetophenone

    Option a – 4-Chloro acetophenone

    Reaction of n-butyl bromide with sodium methoxide produces mainly:

    (A) Isobutane

    (B) Isobutylene

    (C) Sodium tert-butoxide

    (D) n-Butyl methyl ether

    Option d – n-Butyl methyl ether

    Polysubstitution is a major drawback in:

    (A) Reimer Tiemann reaction

    (B) Acetylation of aniline

    (C) Friedel Craft’s acylation

    (D) Friedel Craft’s alkylation

    Option d – Friedel Craft’s alkylation

    Polyhalogen derivative used as antiseptic is:

    (A) Dichloromethane

    (B) Trichloromethane

    (C) Tri-iodomethane

    (D) Tetrachloromethane

    Option c – Tri-iodomethane

    Which of the following alkanes cannot be made in good yield by the Wurtz reaction?

    (A) n-Butane

    (B) n-Hexane

    (C) 2,3-dimethylbutane

    (D) n-Heptane

    Option d – n-Heptane

    Major product formed on the reaction of 2-bromobutane with KOH (alc.) is:

    (A) But-1-ene

    (B) But-2-ene

    (C) Butan-2-ol

    (D) Butan-1-ol

    Option b – But-2-ene

    The optically inactive compound from the following is:

    (A) 2-Chloropentane

    (B) 2-Chloropropanal

    (C) 2-Chloro-2-methylbutane

    (D) 2-Chlorobutane

    Option c – 2-Chloro-2-methylbutane

    IUPAC name of westron is:

    (A) 1,1,2,2-tetrachloroethene

    (B) 1,1,2,2-tetrachloroethane

    (C) 1,2-dichloroethyne

    (D) 1,3,3,3-tetrachloroprop-1-yne

    Option b – 1,1,2,2-tetrachloroethane

    The synthesis of alkyl fluorides is best accomplished by:

    (A) Free radical fluorination

    (B) Sandmeyer’s reaction

    (C) Finkelstein reaction

    (D) Swarts reaction

    Option d – Swarts reaction

    In alkaline hydrolysis of t-butyl bromide, the order of reaction with respect to nucleophile is:

    (A) zero

    (B) first

    (C) pseudo

    (D) second

    Option b – first

    A solution of (-)-1-chloro-1-phenylethane in toluene racemizes slowly in the presence of a small amount of SbCl3 due to the formation of:

    (A) Carbanion

    (B) Carbene

    (C) Carbocation

    (D) Free radical

    Option c – Carbocation

    Iodoform can be prepared from all except:

    (A) Isobutyl alcohol

    (B) Ethyl methyl ketone

    (C) Isopropyl alcohols

    (D) 3-Methyl-2-butanone

    Option a – Isobutyl alcohol

    Which of the following on hydrolysis forms a racemate?

    (A) Chloromethane

    (B) 2-Iodobutane

    (C) 2,-2-Dimethyl propane

    (D) 1-Bromo-1-phenylethane

    Option b – 2-Iodobutane

    Which of the following compounds leads to the formation of a racemate on alkaline hydrolysis?

    (A) 1-Bromo-1-phenyl ethane

    (B) 1-Chloro-3-methyl butane

    (C) Bromo ethane

    (D) 1-Chloro propane

    Option a – 1-Bromo-1-phenyl ethane

    Both geometrical and optical isomerism are exhibited by:

    (A) Dichloro(ethylenediamine)cobalt(III) ion

    (B) Pentaaminechlorocobalt(III)

    (C) Triamminetrichlorocobalt(III) ion

    (D) Trioxalatochromate(III) ion

    Option a – Dichloro(ethylenediamine)cobalt(III) ion

    The effective atomic number of cobalt in the complex is:

    (A) 36

    (B) 33

    (C) 24

    (D) 30

    Option a – 36

    The EAN of iron in potassium ferricyanide is:

    (A) 18

    (B) 35

    (C) 54

    (D) 23

    Option b – 35

    An example of a sigma-bonded organometallic compound is:

    (A) Grignard’s reagent

    (B) Ferrocene

    (C) Cobaltocene

    (D) Ruthenocene

    Option a – Grignard’s reagent

    Which of the following coordination compounds would exhibit optical isomerism?

    (A) trans-dicyanobis(ethylenediamine)chromium(III) chloride

    (B) Tris-(ethylenediamine)cobalt(III)bromide

    (C) Pentaamminenitrocobalt(III)iodide

    (D) Diamminedichloroplatinum(II)

    Option b – Tris-(ethylenediamine)cobalt(III)bromide

    According to IUPAC nomenclature, sodium nitroprusside is named:

    (A) Sodium pentacyanonitrosyl ferrate(III)

    (B) Sodium nitroferricyamide

    (C) Sodium nitroferrocyanide

    (D) Sodium pentacyanonitrosyl ferrate(II)

    Option a – Sodium pentacyanonitrosyl ferrate(III)

    Ligands used in the estimation of hardness of water are:

    (A) EDTA

    (B) DMG

    (C) Chloride

    (D) Bromo

    Option a – EDTA

    Cis-platin is used in the treatment of:

    (A) Malaria

    (B) Cancer

    (C) AIDS

    (D) Yellow fever

    Option b – Cancer

    Which of the following compounds reacts with Lucas reagent on heating to give turbidity and a color change?

    (A) n-propyl alcohol

    (B) isopropyl alcohol

    (C) tert-butyl alcohol

    (D) sec-butyl alcohol

    Option a – n-propyl alcohol

    Primary, secondary, and tertiary alcohols can be distinguished from each other in the laboratory using:

    (A) Finkelstein reagent

    (B) Darzens reagent

    (C) Wurtz reagent

    (D) Lucas reagent

    Option d – Lucas reagent

    Acetonitrile’s functional isomer is:

    (A) methenamine

    (B) Methyl isocyanide

    (C) Methanamide

    (D) Methyl alcohol

    Option b – Methyl isocyanide

    Which of the following pairs is composed of optical isomers?

    (A) n-butyl chloride and isobutyl chloride

    (B) isobutyl chloride and sec-butyl chloride

    (C) secondary butyl chloride and tert-butyl chloride

    (D) d-sec-butyl chloride and l-sec-butyl chloride

    Option d – d-sec-butyl chloride and l-sec-butyl chloride

    When propene is heated with Br2 at 400-600°C, it produces:

    (A) 1,2-dibromopropane

    (B) 2-bromopropane

    (C) allyl bromide

    (D) 1-bromopropane

    Option c – allyl bromide

    Allyl bromide is prepared by the action of N-bromo-succinimide and what?

    (A) Propene

    (B) Ethene

    (C) But-1-ene

    (D) But-2-ene

    Option a – Propene

    During the iodination of a hydrocarbon using mercuric oxide, it is reduced to:

    (A) Alkane (hydrocarbon)

    (B) Water

    (C) Iodine

    (D) Mercuric iodide

    Option d – Mercuric iodide

    The preparation of isopropyl bromide from propene is a:

    (A) Free radical addition reaction

    (B) Electrophilic addition reaction

    (C) Nucleophilic substitution reaction

    (D) Nucleophilic addition reaction

    Option b – Electrophilic addition reaction

    The addition of HBr to α-butylene in the presence of benzoyl peroxide is a:

    (A) Nucleophilic addition reaction

    (B) Free radical substitution reaction

    (C) Electrophilic addition reaction

    (D) Free radical addition reaction

    Option d – Free radical addition reaction

    Isobutyl alcohol is heated with Lucas reagent to form

    (A) Isobutyl chloride

    (B) sec.butyl chloride

    (C) tert.butyl chloride

    (D) isopropyl chloride

    Option c – tert.butyl chloride

    Markonikov’s rule is followed by the addition of ……. an alkene under normal conditions.

    (A) HCl

    (B) HBr

    (C) HI

    (D) All of the above

    Option d – All of the above

    Mayo effect can be observed in which of the following reactions?

    (A) Hydrogenation of alkene

    (B) Halogenation of alkane

    (C) Hydrohalogenation of alkene

    (D) Williamson synthesis

    Option c – Hydrohalogenation of alkene

    During the chlorination of methyl benzene, the major product obtained is

    (A) p-Chloro toluene

    (B) 2-chloro toluene

    (C) m-Chloro toluene

    (D) o-chloro toluene

    Option a – p-Chloro toluene

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