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Chapter Wise Test Series for NEET

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Chapter Wise Test Series for NEET. We covered all the Chapter Wise Test Series for NEET Students in this post for free so that you can practice well for the exam.

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We have divided the complete NEET syllabus into several small posts on our website for your convenience. You will get their respective links in the related posts section provided below.

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MCQ on Biomolecules for NEET Students

Assertion: Propan-1-ol is less soluble in water than methanol. Reason: With the increase in the size of the alkyl group, the solubility of the alcohols decreases.

(A) Assertion and Reason are true. The reason is the correct explanation of the Assertion.

(B) Assertion and Reason are true. The reason is not the correct explanation of the Assertion.

(C) The assertion is true, and the Reason is false.

(D) The assertion is false, Reason is true.

Option a – Assertion and Reason are true. The reason is the correct explanation of the Assertion.

Which of the following properties/characteristics are different for the compounds (+) 2-butanol and (-) 2-butanol? (I) Solubility in water (II) Specific rotation (III) Spatial arrangement around the chirality center (IV) Angle around the chirality center (V) Refractive index (VI) Reaction with sodium metal

(A) I, II, VI

(B) II, III

(C) III, IV, V

(D) I, III, IV

Option b – II, III

The common name of 1-bromo-2-methylpropane is ……..

Which State of India experiences the maximum annual variation of rainfall?

(A) Meghalaya

(B) Kerala

(C) Rajasthan

(D) West Bengal

Show Answer

(A) tert-butyl bromide

(B) sec-butyl bromide

(C) isobutyl bromide

(D) n-butyl bromide

Option c – isobutyl bromide

Which of the following conversion (single step) can be carried out by Swarts reaction?

(A) Chloroethane → Fluoroethane

(B) Chloroethane → Iodoethane

(C) Ethanol → Chloroethane

(D) Ehanol → Bromoethane

Option a – Chloroethane → Fluoroethane

On heating phenyl methyl ether with HI, ……… are formed.

Pakyong Airport is located in?

(A) Sikkim

(B) Jammu and Kashmir

(C) Arunachal Pradesh

(D) Mizoram

Show Answer

(A) iodobenzene and iodomethane

(B) phenol and iodomethane

(C) benzene and methanol

(D) phenol and methanol

Option b – phenol and iodomethane

……….. CANNOT be used as a starting material for the preparation of iodoform by using iodine and sodium hydroxide.

(A) Ethyl methyl ketone

(B) Isopropyl alcohol

(C) Acetaldehyde

(D) Isobutyl alcohol

Option d – Isobutyl alcohol

Sodium benzene sulphonate fused with sodium hydroxide forms ………. on acidic hydrolysis.

(A) benzene sulphonic acid

(B) benzoic acid

(C) phenol

(D) pyrogallol

Option c – phenol

Choose the CORRECT statement(s) from the following : (I) The C-X bond length is longer in chloromethane as compared to bromomethane. (II) The C-X bond length is longer in bromobenzene as compared to bromomethane. (III) The C-X bond length is longer in chloromethane as compared to chlorobenzene.

(A) Only (I)

(B) Only (III)

(C) (I) and (II)

(D) (II) and (III)

Option b – Only (III)

When propyne is treated with aqueous H₂SO4 in the presence of HgSO4, the product obtained is ………

(A) CH3 -CH2 – CHO

(B) CH3-CH2 – CO – CH3

(C) CH3 – CO – CH3

(D) CH3 – CH₂ – CH₂ – OH

Option c – CH3 – CO – CH3

One mole of compound ‘X’ on catalytic hydrogenation gives two moles of primary alcohol (Y). Identify ‘X’.

(A) Propanone

(B) Ethyl propanoate

(C) Propanal

(D) Propyl propanoate

Option d – Propyl propanoate

Aldehydes or ketones when treated with C6H5 – NH – NH₂, the product formed is ……….

(A) semicarbazone

(B) phenylhydrazone

(C) hydrazone

(D) oxime

Option b – phenylhydrazone

The conversion shown below can be carried out by using which of the following reagents? CH3CH₂CH=CH₂ -> CH3CH₂CH₂CH₂OH

(A) Conc. H₂SO4 and then heating with H₂0

(B) BH3/THF and then H₂O2, NaOH

(C) Alcoholic NaOH

(D) Moist Ag₂O

Option b – BH3/THF and then H₂O2, NaOH

Assertion p-Aminophenol is less acidic than phenol. Reason: Electron-donating groups do not favor the formation of phenoxide ions.

(A) Assertion and Reason are true. The reason is the correct explanation of the Assertion.

(B) Assertion and Reason are true. The reason is not the correct explanation of the Assertion.

(C) The assertion is true. The reason is false.

(D) The assertion is false. The reason is true.

Option a – Assertion and Reason are true. The reason is the correct explanation of the Assertion.

When phenol is heated with a nitrating mixture, it forms a compound (X). Which of the following group is NOT present in compound (X)? (I)-CHO (II) -NO₂ (III) -COOH (IV)−NH, (V) -OH

(A) (I) and (II)

(B) (I) and (IV)

(C) (II), (III) and (IV)

(D) (I), (III), and (IV)

Option d – (I), (III), and (IV)

Compound (X) undergoes alkaline hydrolysis by SN1 route to form ‘Y’ and ‘Z’ in equal proportion. ‘Y’ and ‘Z’ are enantiomers and the final reaction mixture is racemic. Identify compound (X).

(A) 2-Bromo-2-methylpropane

(B) 1-Bromo-1-phenylethane

(C) 2-Bromopropane

(D) 1-Bromo-2-phenylpropane

Option b – 1-Bromo-1-phenylethane

Which of the following is allylic alcohol? ( Chapter Wise Test Series for NEET )

(A) 2-Phenylpropan-2-ol

(B) 2-Methylpropan-2-ol

(C) Prop-1-en-1-ol

(D) 2-Methylbut-3-en-2-ol

Option d – 2-Methylbut-3-en-2-ol

In which of the following molecules, all the carbon atoms are sp² hybridized?

(A) Acetaldehyde

(B) Acrolein

(C) Glyceraldehyde

(D) Crotonaldehyde

Option b – Acrolein

When an organic compound (X) is treated with carbon monoxide and HCl under high pressure in the presence of a catalyst (Anhy. AlCl3 + Cu₂Cl₂), another organic compound (Y) is obtained. Compound (Y) is heated with alkaline KMnO4 to obtain benzoic acid. Compound (Y) gives a positive result with Schiff reagent but a negative result with Fehling solution. Identify (X) and (Y) respectively.

(A) X= Benzene; Y = Benzophenone

(B) X = Toluene; Y = Benzaldehyde

(C) X = Benzene; Y = Benzaldehyde

(D) X = Benzene; Y = Acetophenone

Option c – X = Benzene; Y = Benzaldehyde

We covered all the biomolecules neet mcq above in this post for free so that you can practice well for the exam.

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