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NEET • CHEMISTRY • ORGANIC CHEMISTRY-SOME BASIC PRINCIPLES AND TECHNIQUES

Organic chemistry-some basic principles and techniques practice · Mixed difficulty

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211 Medium
211 of 392
Application +4 | -1
An enantiomerically pure acid is treated with racemic mixture of an alcohol having one chiral carbon. The ester formed will be
View answer and explanation
Correct option: A
Optically active mixture
Option A (Optically active mixture) is correct because the reaction of an enantiomerically pure acid with a racemic alcohol produces a mixture of diastereomeric esters, which are optically active.
212 Easy
212 of 392
Remembering +4 | -1
Fractional distillation is useful in distillation of
View answer and explanation
Correct option: D
All of these
Option D (All of these) is correct because fractional distillation is used to separate components in petroleum, coal-tar, and crude alcohol based on their boiling points.
213 Hard
213 of 392
Understanding +4 | -1
How will you separate a solution (miscible) of benzene +CHCl3+{CHCl}_3 ?
View answer and explanation
Correct option: C
distillation
Option C is correct because benzene and chloroform are miscible liquids with different boiling points, making distillation the appropriate separation technique.
214 Hard
214 of 392
Understanding +4 | -1
Which of the following is ambident nucleophile
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Correct option: D
All
Option D (All) is correct because ambident nucleophiles are nucleophiles that can attack from two or more different sites, and all listed options (NH2OH, NCO-, NO2-) exhibit this behavior.
215 Easy
215 of 392
Understanding +4 | -1
Geometrical isomerism is possible in case of
View answer and explanation
Correct option: A
Pentene-2
Option A (Pentene-2) is correct because geometrical isomerism requires restricted rotation around a double bond and two different groups on each carbon of the double bond, which pentene-2 fulfills.
216 Medium
216 of 392
Application +4 | -1
CH3−C≡CH+HOH→Hg2+/H2SO4AC{H_3} - C \equiv CH + HOH\xrightarrow{{H{g^{2 + }}/{H_2}S{O_4}}}A
The number of sigma and pi bonds that are present in the molecule AA
View answer and explanation
Correct option: A
9 sigma and 1 pi
Option A (9 sigma and 1 pi) is correct because the product A is CH3COCH3 (acetone), which has 9 sigma bonds and 1 pi bond.
217 Medium
217 of 392
Remembering +4 | -1
Fischer projection indicates :
View answer and explanation
Correct option: A
Horizontal substituents above the plane
Option A (Horizontal substituents above the plane) is correct because, in Fischer projections, horizontal lines represent bonds projecting out of the plane (towards the viewer).
218 Easy
218 of 392
Understanding +4 | -1
Which of the following sodium compound/compounds are formed when an organic compound containing both nitrogen and sulphur is fused with sodium?
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Correct option: B
Thiocyanate
Option B (Thiocyanate) is correct because when an organic compound containing both nitrogen and sulfur is fused with sodium, it forms sodium thiocyanate (NaSCN).
219 Medium
219 of 392
Analyzing +4 | -1
Which of the following compound will give white precipitate on heating with HNO3{HNO}_3 followed by addition of silver nitrate?
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Correct option: C
Both (1) and (2)
Option C (Both (1) and (2)) is correct because both compounds contain chlorine that can be converted to chloride ions, which then react with silver nitrate to form a white precipitate of silver chloride.
220 Medium
220 of 392
Analyzing +4 | -1
An organic compound A is oxidised with Na2O2N{a_2}{O_2} followed by boiling with HNO3HN{O_3}. The resultant solution is then treated with ammonium molybdate to yield a yellow precipitate. Based on above observation, the element present in the given compound is
View answer and explanation
Correct option: B
Phosphorus
Option B (Phosphorus) is correct because the yellow precipitate with ammonium molybdate indicates the presence of phosphorus.
221 Hard
221 of 392
Understanding +4 | -1
Assertion (A): Components of a mixture of red and blue inks can be separated by distributing the components between stationary and mobile phases in paper chromatography.

Reason (R): The coloured components of inks migrate at different rates because paper selectively retains different components according to the difference in their partition between two phases.
View answer and explanation
Correct option: A
Both A\mathrm{A} and R\mathrm{R} are correct ; R\mathrm{R} is the correct explanation of AA.
Option A is correct because both the assertion and reason are true, and the reason correctly explains why components of a mixture of inks can be separated by paper chromatography.
222 Easy
222 of 392
Understanding +4 | -1
Which of the following intermediate have the complete octet around the carbon atom?
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Correct option: B
Carbanion
Option B (Carbanion) is correct because a carbanion has 8 electrons around the carbon atom, fulfilling the octet rule.
223 Easy
223 of 392
Understanding +4 | -1
Inductive effect involves
View answer and explanation
Correct option: B
partial displacement of σ\sigma electrons
Option B (partial displacement of σ\sigma electrons) is correct because the inductive effect involves the partial displacement of sigma electrons along a chain of atoms.
224 Easy
224 of 392
Analyzing +4 | -1
Strongest acid among the following
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Correct option: C
CF3COOHC{F_3}COOH
Option C (CF3COOHC{F_3}COOH) is the strongest acid because the three fluorine atoms, being highly electronegative, exert a strong electron-withdrawing inductive effect (-I effect) that significantly stabilizes the conjugate base (carboxylate ion), thus increasing the acidity of the carboxylic acid.
225 Easy
225 of 392
Analyzing +4 | -1
The compound having molecular formula C4H10O{\mathrm{C}_4}{\mathrm{H}_{10}}\mathrm{O} can show :
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Correct option: D
All of these
Option D (All of these) is correct because C4H10O{\mathrm{C}_4}{\mathrm{H}_{10}}\mathrm{O} can exhibit metamerism, functional isomerism, and positional isomerism.
226 Medium
226 of 392
Application +4 | -1
The number of σ−  and  π - \sigma - \,\,{\text{and}}\,\,\pi {\text{ - }} bonds in but-1-ene- 3-yne are:
View answer and explanation
Correct option: B
7σ  and  3π7\sigma \,\,{\text{and}}\,\,3\pi
Option A (Allyl carbonium ion (CH2=CH−C+H2)(C{H_2} = CH - \mathop {\mathrm{ }C}\limits^ + {H_2}) is more stable then propyl carbonium ion) is correct because the allyl carbocation is stabilized by resonance, while the propyl carbocation is not.
227 Medium
227 of 392
Analyzing +4 | -1
Which of the following is most reactive towards elimination reaction?
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Correct option: D
RO−R{\mathrm{O}^ - }
Option D (RO−RO^−) is the most reactive towards elimination because alkoxides are strong bases and favor elimination reactions.
228 Medium
228 of 392
Understanding +4 | -1
Na2S+Na2[Fe(CN)5NO]\mathrm{N}{\mathrm{a}_2}\mathrm{S} + \mathrm{N}{\mathrm{a}_2}\left[ {\mathrm{Fe}{{\left( {\mathrm{CN}} \right)}_5}\mathrm{NO}} \right] →\to Purple colour. It is due to
View answer and explanation
Correct option: D
Na4[Fe(CN)5NOS]\mathrm{N}{\mathrm{a}_4}\left[ {\mathrm{Fe}{{\left( {\mathrm{CN}} \right)}_5}\mathrm{NOS}} \right]
Option D (Na4[Fe(CN)5NOS]\mathrm{N}{\mathrm{a}_4}\left[ {\mathrm{Fe}{{\left( {\mathrm{CN}} \right)}_5}\mathrm{NOS}} \right]) is correct because the purple color in the test for both nitrogen and sulfur is due to the formation of sodium nitroprusside, Na4[Fe(CN)5NOS]Na_4[Fe(CN)_5NOS].
229 Medium
229 of 392
Remembering +4 | -1
IUPAC name of C6H5CN{C_6}{H_5}CN is:
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Correct option: B
Benzene nitrile
Option B (Benzene nitrile) is correct because it accurately reflects the IUPAC nomenclature for a benzene ring directly bonded to a nitrile group.
230 Easy
230 of 392
Application +4 | -1
The correct IUPAC name of CH3CH−C≡C−CH3\mathrm{CH}_3 \mathrm{CH}-\mathrm{C} \equiv\mathrm{C}-\mathrm{CH}_3 is:
View answer and explanation
Correct option: C
4-methyl hex-2-yne
Option B (RS⊖R{S^ \ominus } is less basic but more nucleophilic than RO ⊖R{O^{\, \ominus }}) is correct because sulfur is larger and more polarizable than oxygen, making the thiolate anion a better nucleophile but a weaker base.
231 Easy
231 of 392
Remembering +4 | -1
Which of the following statements is wrong?
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Correct option: C
Organic compounds cannot be synthesized in the laboratory
Option C (Organic compounds cannot be synthesized in the laboratory) is wrong because Wöhler's synthesis of urea disproved this statement, showing that organic compounds can indeed be synthesized in the lab.
232 Medium
232 of 392
Application +4 | -1
Compound (A) is formed on treating a benzilwith NaBH4\mathrm{NaBH}_4. The number of possible meso isomers for (A) are
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Correct option: A
1
Option A (1) is correct because the reduction of benzil with NaBH4 produces a diol, and only one meso isomer is possible due to the symmetry of the molecule.
233 Easy
233 of 392
Understanding +4 | -1
The suitable method for separation of a mixture of ortho and para nitrophenols is
View answer and explanation
Correct option: D
steam distillation
Option D is correct because ortho and para nitrophenols have different volatilities due to intramolecular hydrogen bonding in ortho-nitrophenol, allowing separation by steam distillation.
234 Easy
234 of 392
Remembering +4 | -1
Lactic acid is:
View answer and explanation
Correct option: C
α−\alpha - hydroxypropanoic acid
Option C (α−\alpha - hydroxypropanoic acid) is correct because lactic acid has a hydroxyl group attached to the alpha carbon of propanoic acid.
235 Hard
235 of 392
Application +4 | -1
0.5 g of an organic compound containing nitrogen on Kjeldahlising required 29 mL of N/5H2SO4N/5{\mathrm{H}_2}\mathrm{S}{\mathrm{O}_4} for complete neutralization of ammonia. The percentage of nitrogen in the compound is:
View answer and explanation
Correct option: B
16.216.2
Option B (16.216.2) is correct because the percentage of nitrogen is calculated using the volume and molarity of the sulfuric acid used to neutralize the ammonia.
236 Medium
236 of 392
Application +4 | -1
The conversion of propan-1-ol to n-butylamine involves the sequential addition of reagents. The correct sequential order of reagents is
View answer and explanation
Correct option: A
(i)  SOCl2  (ii)  KCN  (iii)H2/Ni,Na(Hg)/C2H5OH({\text{i}})\,\,SOC{l_2}\,\,({\text{ii}})\,\,KCN\,\,({\text{iii}}){H_2}/Ni,Na(Hg)/{C_2}{H_5}OH
Option A ((i) SOCl2 (ii) KCN (iii)H2/Ni,Na(Hg)/C2H5OH)(({\text{i}})\,SOC{l_2}\,({\text{ii}})\,KCN\,({\text{iii}}){H_2}/Ni,Na(Hg)/{C_2}{H_5}OH) is correct because it outlines the correct sequence of reactions: converting the alcohol to an alkyl chloride using SOCl2, followed by nucleophilic substitution with KCN to form a nitrile, and finally reduction of the nitrile to an amine using H2/Ni or Na(Hg)/C2H5OH.
237 Hard
237 of 392
Analyzing +4 | -1
An organic compound contains 46.78%46.78 \% of a halogen X{X}. When 2.00 g2.00 \mathrm{~g} of this compound is heated with fuming HNO3{HNO}_3 in the presence of AgNO3,2.21g  AgX{AgNO}_3, 2.21 \mathrm{g} \,\,{AgX} was formed. The halogen X{X} is [Given: atomic weight of Ag=108,F=19,Cl=35.5,Bi=80,I=127]{Ag}=108, {F}=19, {Cl}=35.5, {Bi}=80, {I}=127]
View answer and explanation
Correct option: C
BrBr
Option C (Br) is correct because the molar mass calculated from the given data matches the molar mass of bromine.
238 Easy
238 of 392
Understanding +4 | -1
Which among the following is not electrophile
View answer and explanation
Correct option: A
C⊕H5\mathop C\limits^ \oplus {H_5}
Option A (C⊕H5\mathop C\limits^ \oplus {H_5}) is correct because CH5+CH_5^+ is not a typical electrophile due to its structure and bonding; it is a hypercoordinated carbocation.
239 Easy
239 of 392
Analyzing +4 | -1
Assertion (A) : SO3\mathrm{SO}_3 is a nucleophile.

Reason (R): SO3\mathrm{SO}_3 has lone-pair of electrons.
View answer and explanation
Correct option: D
A\mathbf{A} and R\mathbf{R} both are false.
Option D (A and R both are false) is correct because SO3 is an electrophile, not a nucleophile, and it does not have a lone pair of electrons.
240 Easy
240 of 392
Remembering +4 | -1
Mesomeric effect is due to
View answer and explanation
Correct option: B
Delocalisation of π\pi electrons
Option B (Delocalisation of π\pi electrons) is correct because the mesomeric effect involves the delocalization of pi electrons or lone pairs of electrons in a conjugated system.
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