Which of the following compound will most easily be attacked by an electrophile?
A.Chlorobenzene
Electrophilic Substitution
B.Toluene
Electrophilic Substitution
C.Benzoic acid
Electrophilic Substitution
D.Phenol
Electrophilic Substitution
Solution & Explanation
### Core Logic
An electrophile seeks electrons. Higher electron density in the benzene ring makes it more susceptible (reactive) to electrophilic attack. The ring's electron density is governed by the inductive (I) and mesomeric/resonance (M) effects of the attached groups.
### Step 1: Evaluate Substituent Effects
- Cl$Cl$ (in chlorobenzene): shows weak +M effect but strong -I effect, causing net deactivation.
- CH_3$CH_3$ (in toluene): shows +I effect and hyperconjugation, slightly activating the ring.
- COOH$COOH$ (in benzoic acid): shows strong -M and -I effect, highly deactivating.
- OH$OH$ (in phenol): shows strong +M effect which dominates its weak -I effect, strongly activating the ring.
### Step 2: Conclusion
Phenol has the highest electron density in the ring among the given options due to the strong +M effect of the -OH group. Thus, it is most easily attacked by an electrophile.
### Pattern Recognition
Reactivity towards Electrophilic Aromatic Substitution (EAS):
Strong +M (-OH, -NH2) > Weak +I/Hyperconjugation (-CH3) > Halogens (-Cl, net deactivating) > Strong -M (-COOH, -NO2).
### Evaluation Rubric / Model Answer
null
### Chapter Mix
Class 11 Chemistry: Hydrocarbons
Class 12 Chemistry: Alcohols, Phenols and Ethers
Keywords:#electrophile attack on benzene#JEE Main 2024 Morning Q72#Alcohols, Phenols and Ethers JEE Main 2024#Electrophilic Substitution JEE Main 2024
More Alcohols, Phenols and Ethers Previous-Year Questions — Page 3
Q66jee_main_2024_30_january_eveningPreparation of Alcohols
Product A and B formed in the following set of reactions are:
The diagram shows a reaction pathway for synthesizing product A and B.
A.textA = mathrmCH_2OH text, B = mathrmCH_2OH$\text{A = } \mathrm{CH_2OH} \text{, B = } \mathrm{CH_2OH}$
B.textA = mathrmCH_3OH text, B = mathrmCH_3OH$\text{A = } \mathrm{CH_3OH} \text{, B = } \mathrm{CH_3OH}$
C.textA = mathrmCH_2OH text, B = mathrmCH_3OH$\text{A = } \mathrm{CH_2OH} \text{, B = } \mathrm{CH_3OH}$
D.textA = mathrmCH_3OH text, B = mathrmCH_3OH$\text{A = } \mathrm{CH_3OH} \text{, B = } \mathrm{CH_3OH}$
Solution
### Core Logic
The given substrate is an alkene attached to a benzene ring (styrene derivative).
Reaction 1: Acid-catalyzed hydration (H^+ / H_2O$H^+ / H_2O$)
This proceeds via Markovnikov's rule. The proton attacks the alkene to form the most stable carbocation (benzyllic and secondary). Water then attacks this carbocation to yield the alcohol at the substituted position (product A: Ph-CH(OH)-CH_3$Ph-CH(OH)-CH_3$).
Reaction 2: Hydroboration-Oxidation (B_2H_6$B_2H_6$, then H_2O_2/NaOH$H_2O_2/NaOH$)
This proceeds via anti-Markovnikov addition of water across the double bond without carbocation rearrangement. The OH$OH$ group adds to the less substituted carbon atom of the alkene (product B: Ph-CH_2-CH_2-OH$Ph-CH_2-CH_2-OH$).
The diagram shows a reaction pathway for synthesizing product A and B.
### Pattern Recognition
H^+/H_2O$H^+/H_2O$ = Markovnikov hydration (carbocation intermediate).
B_2H_6 / H_2O_2, OH^-$B_2H_6 / H_2O_2, OH^-$ = Anti-Markovnikov hydration (concerted, no rearrangement).
### Evaluation Rubric / Model Answer
null
### Chapter Mix
Class 12 Chemistry: Alcohols Phenols and Ethers
Class 11 Chemistry: Hydrocarbons
Q69jee_main_2024_31_jan_morningChemical Reactions of Alcohols
Given below are two statements: One is labelled as Assertion A and the other is labelled as Reason R:
Assertion A: Alcohols react both as nucleophiles and electrophiles.
Reason R: Alcohols react with active metals such as sodium, potassium and aluminum to yield corresponding alkoxides and liberate hydrogen.
In the light of the above statements, choose the correct answer from the options given below:
A.textA is false but R is true.$\text{A is false but R is true.}$
B.textA is true but R is false.$\text{A is true but R is false.}$
C.textBoth A and R are true and R is the correct explanation of A.$\text{Both A and R are true and R is the correct explanation of A.}$
D.textBoth A and R are true but R is NOT the correct explanation of A.$\text{Both A and R are true but R is NOT the correct explanation of A.}$
Solution
### Core Logic
Assertion (A) is correct. Alcohols can act as nucleophiles (in reactions involving O-H bond cleavage) and as electrophiles (in reactions involving C-O bond cleavage after protonation).
Reason (R) is correct. Alcohols react with active metals to form alkoxides and H_2$H_2$ gas.
However, Reason (R) only explains the acidic nature of the O-H bond (which relates to nucleophilic behavior when broken) but does not explain the electrophilic behavior (C-O cleavage). Thus, (R) is not the correct explanation for (A).
### Evaluation Rubric / Model Answer
null
### Chapter Mix
Class 12 Chemistry: Alcohols, Phenols and Ethers
Q74jee_main_2024_31_jan_morningAcidity of Phenols
Given below are two statements: One is labelled as Assertion A and the other is labelled as Reason R:
Assertion A: pK_a$pK_a$ value of phenol is 10.0 while that of ethanol is 15.9.
Reason R: Ethanol is stronger acid than phenol.
In the light of the above statements, choose the correct answer from the options given below:
A.textA is true but R is false.$\text{A is true but R is false.}$
B.textA is false but R is true.$\text{A is false but R is true.}$
C.textBoth A and R are true and R is the correct explanation of A.$\text{Both A and R are true and R is the correct explanation of A.}$
D.textBoth A and R are true but R is NOT the correct explanation of A.$\text{Both A and R are true but R is NOT the correct explanation of A.}$
Solution
### Core Logic
Assertion A is true: Phenol has a pK_a$pK_a$ of around 10.0, and ethanol has a pK_a$pK_a$ of around 15.9.
Reason R is false: A lower pK_a$pK_a$ value implies higher acidity. Therefore, phenol is a stronger acid than ethanol. This is because the conjugate base of phenol (phenoxide ion) is resonance-stabilized, whereas the ethoxide ion is destabilized by the +I effect of the ethyl group.
### Evaluation Rubric / Model Answer
null
### Chapter Mix
Class 12 Chemistry: Alcohols, Phenols and Ethers
More Alcohols, Phenols and Ethers Questions — jee_main_2024_01_february_morning
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