Basic Principles of Orgainc Chemistry MCQs for NEET — Chemistry Questions with Answers

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With respect to the conformers of ethane, which of the following statements is true?

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Explanation

(d) Isomers which are possible by rotation about single bonds without cleavage of any bond are called conformers. In ethane, an infinite number of conformations are possible. There are two extreme forms, the staggered conformation, which is the most stable and the eclipsed conformation which is least stable. Among the conformers of ethane, bond angle and bond length remain same while their energy, stability and dihedral angle are different.

Which one is the correct order of acidity?

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Explanation

(b) Greater the s-character of C-atom in hydrocarbons, greater the electronegativity of

that carbon and thus greater the acidic nature of the H attached to electronegative carbon.

                        CH≡CH CH2=CH2 CH3-CH3

Hybridisation:         sp        sp2        sp3

s-character:          50%      33%       25%

Electronegativity:     â†Max.---------------------------------------

Acidic character      â†Max.---------------------------------------

of terminal H

Thus, CH≡CH > CH3C≡CH > CH2=CH2 > CH3-CH3

The correct statement regarding the comparison of staggered and eclipsed conformations of ethane,is

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Explanation

The staggered conformation of ethane is more stable than the eclipsed conformation because it has no torsional strain. In the staggered conformation, the hydrogen atoms are arranged in a way that minimizes the steric repulsion between them, resulting in lower potential energy.

Some meta-directing substituents in aromatic substitution are given. Which one is most deactivating?

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Among the following compounds the one that is most reactive towards electrophilic nitration is

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Explanation

Toluene is the most reactive towards electrophilic nitration among the given options. The methyl group being an electron-donating substituent activates the benzene ring, making it more susceptible to electrophilic attack by the nitro group.

The correct order of decreasing acid strength of trichloroacetic acid (A), trifluoroacetic acid (B), acetic acid (C) and formic acid (D) is

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Explanation

The correct order of decreasing acid strength is: trifluoroacetic acid (B) > trichloroacetic acid (A) > formic acid (D) > acetic acid (C). The highly electronegative fluorine and chlorine atoms withdraw electrons, making the respective acids stronger than acetic and formic acids.

Which of the following does not exhibit optical isomerism?

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Among the given compounds, the most susceptible to nucleophilic attack at the carbonyl group is

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Explanation

(d) Key Idea Lesser the electron density of acyl carbon atom, more will be the susceptibility of nucleophile to attack it.

The Cl atom has strong -I effect and weakest +R effect because of the weak p-bond between the small sized C-atom and large sized Cl atom.

Thus, in CH3COCl, acyl carbon has least electron density and hence, more susceptible for nucleophilic attack.

The IUPAC name of the compound having the formula CHC-CH=CHis

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Explanation

(d) Double bond have preference over triple bond while naming CHC-CH=CH2
                                                                                       1-butene 3-yne

The relative reactivates of acyl compounds towards nucleophilic substitution are in the order of

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