Inductive, electromeric, resonance and hyperconjugation effects — practice questions
32 questions in the bank on this idea. Below are 10 of them, exactly as they appear in a test.
List-I Reaction List-I Mechanism A. Williamson Synthesis I. Electrophilic addition B. Friedel Craft Reaction II. Free radical substitution C. Bromination of vinyl benzene III. Nucleophilic substitution D. Chlorination of toluene in light IV. Electrophilic substitution Choose the correct answer from the options given below:
- A. A-III, B-I, C-II, D-IV
- B. A-III, B-IV, C-II, D-I
- C. A-III, B-IV, C-I, D-II
- D. Â A-I, B-III, C-IV, D-II
Increasing order of electron withdrawing power of following functional groups is : a. -CN b. -COOH c. d. -I
- A.
- B.
- C.
- D.
Identify the correct statements : The presence of –NO 2 group in benzene ring A. activates the ring towards electrophilic substitutions. B. deactivates the ring towards electrophilic substitutions. C. activates the ring towards nucleophilic substitutions. D. deactivates the ring towards nucleophilic substitutions. Choose the correct answer from the options given below :
- A. A and D Only
- B. B and D Only
- C. C and A Only
- D. B and C Only
Identify correct statement/s : (A) and are activating group. (B) and -OH are meta directing group. (C) -CN and are meta directing group. (D) Activating groups act as ortho - and para directing groups. (E) Halides are activating groups. Choose the correct answer from the options given below :
- A. and (D) only
- B. and only
- C. (A) and (C) only
- D. (A) only
Match List I with List II : LIST I Mechanism steps LIST II Effect A. I. E effect B. II. R effect C. III. E effect D. IV. R effect Choose the correct answer from the options given below :
- A. (A) - (I), (B) - (II), (C) - (IV), (D) - (III)
- B. (A) - (II), (B) - (IV), (C) - (III), (D) - (I)
- C. (A) - (III), (B) - (I), (C) - (II), (D) - (IV)
- D. (A) - (IV), (B) - (III), (C) - (I), (D) - (II)
The functional group that shows negative resonance effect is :
- A.
- B.
- C.
- D.
Ionic reactions with organic compounds proceed through : (A) homolytic bond cleavage (B) heterolytic bond cleavage (C) free radical formation (D) primary free radical (E) secondary free radical Choose the correct answer from the options given below :
- A. (A) only
- B. (B) only
- C. (C) only
- D. (D) and (E) only
The interaction between bond and lone pair of electrons present on an adjacent atom is responsible for
- A. Resonance effect
- B. Electromeric effect
- C. Hyperconjugation
- D. Inductive effect
Resonance in carbonate ion is Which of the following is true?
- A. It is possible to identify each structure individually by some physical or chemical method.
- B. All these structures are in dynamic equilibrium with each other.
- C. Each structure exists for equal amount of time.
- D. has a single structure i.e., resonance hybrid of the above three structures.
Given below are two statements, one is labelled as Assertion A and the other is labelled as Reason R Assertion A : Benzene is more stable than hypothetical cyclohexatriene Reason R : The delocalised electron cloud is attracted more strongly by nuclei of carbon atoms. In the light of the above statements, choose the correct answer from the options given below:
- A. A is true but R is false
- B. Both A and R are correct and R is the correct explanation of A
- C. Both A and R are correct but R is NOT the correct explanation of A
- D. A is false but R is true
Want to know which of these you would get wrong?
Reading a question and answering it under a clock are different things. Take the 20-question diagnostic and see where the marks actually go.
Start the diagnostic →