0
question_answer1) Directions : (1 - 15) For question numbers 1-15, a statement of assertion followed by a statement of reason is given. Choose the correct answer out of the following choices. Assertion: p-Dichlorobenzene is less soluble in organic solvents than the corresponding o-isomer. Reason: o-Dichlorobenzene is polar while p-dichlorobenzene is not.
question_answer2) Assertion: Boiling point of alkyl halides increases with increase in molecular weight. Reason: Boiling point of alkyl halides is in the order\[RI\text{ }>\text{ }RBr\text{ }>\text{ }RCI\text{ }>RF\].
question_answer3) Assertion: Tertiary haloalkanes are more reactive than primary haloalkanes towards elimination reactions. Reason: The +I effect of the alkyl groups weakens the C - X bond.
question_answer4) Assertion: Vinylic halides are highly reactive towards nucleophilic substitution reactions. Reason: Reactivity is due to the polarity of carbon-halogen bond.
question_answer5) Assertion: The presence of nitro group facilitates nucleophilic substitution reactions in aryl halides. Reason: The intermediate carbanion is stabilised due to the presence of nitro group.
question_answer6) Assertion: Lower members of alkyl halides are colourless gases. Reason: Alkyl iodides in general turn black on exposure to air and light.
question_answer7) Assertion: Boiling point of RCI is greater than RF. Reason: R-CI is more stable than R-F.
question_answer8) Assertion: Bromobenzene upon reaction with \[B{{r}_{2}}/Fe\] gives 1, 4-dibromobenzene as the major product. Reason: In bromobenzene, the inductive effect of the bromo group is more dominant than the mesomeric effect in directing the incoming electrophile.
question_answer9) Assertion: Electron withdrawing groups in aryl halides decrease the reactivity towards nucleophilic substitution. Reason: 2, 4-Dinitrochlorobenzene is more reactive than chlorobenzene.
question_answer10) Assertion: Benzyl chloride is more reactive thanp-chlorotoluene towards aqueous NaOH. Reason: The C - Cl bond in benzyl chloride is more polar than C - Cl bond inp-chlorotoluene.
question_answer11) Assertion: 2-Chloro-3-methylbutan on treatment with alcoholic potash give 2-methylbut-2-ene as major product. Reason: The reaction occurs according to Saytzeff rule.
question_answer12) Assertion: Haloalkanes show H-bonding. Reason: Haloalkanes are insoluble in water.
question_answer13) Assertion: Vinyl chloride is less reactive than alkyl chloride. Reason: Stability of alkyl halide decreases as the strength of C-X bond decreases.
question_answer14) Assertion: Aryl halide gives a mixture of o-and p-products. Reason: Aryl halides undergo electrophilic substitutions more readily than benzene.
question_answer15) Assertion: Carbon-halogen bond in aryl halide has partial double bond character. Reason: Aryl halides undergo nucleophilic substitution easily.
Please Wait you are being redirected....
You need to login to perform this action.You will be redirected in 3 sec
OTP has been sent to your mobile number and is valid for one hour
Your mobile number is verified.