(a)
(b)
(c)
(d)
Ans: (b)
Q2: Which one of the following alcohols reacts instantaneously with Lucas reagent? (NEET 2024)
(a)
(b)
(c)
(d)
Ans: (d)
Tertiary alcohols react instantaneously with Lucas reagent and gives immediate turbidity. In case of tertiary alcohols, they form halides easily with Lucas reagent (conc. HCl and ZnCl2)
Q3: Intramolecular hydrogen bonding is present in (NEET 2024)
(a)
(b)
(c)
(d) HF
Ans: (a)
In o-nitrophenol intramolecular H-bonding is present.
Q4: Major products A and B formed in the following reaction sequence, are (NEET 2024)
(a)
(b)
(c)
(d)
Ans: (a)
(a)
(b)
(c)
(d)
Ans: (d)
Q2: Consider the following reaction (NEET 2023)
Identify products A and B :-
(a)
(b)
(c)
(d)
Ans: (b)
Q3: Which amongst the following will be most readily dehydrated under acidic conditions? (NEET 2023)
(a)
(b)
(c)
(d)
View AnswerAns: (a)
Due to presence of conjugation in product.
Q1: Match the reagents (List-I) with the product (List-II) obtained from phenol. (NEET 2022 Phase 2)
Choose the correct answer from the options given below :
(a) (a) - (iv), (b) - (ii), (c) - (i), (d) - (iii)
(b) (a) - (iii), (b) - (iv), (c) - (i), (d) - (ii)
(c) (a) - (ii), (b) - (i), (c) - (iv), (d) - (iii)
(d) (a) - (iv), (b) - (iii), (c) - (ii), (d) - (I)
Ans: (d)
Q2: Which one of the following reaction sequence is incorrect method to prepare phenol? (NEET 2022 Phase 2)
(a)
(b) Aniline, NaNO2 + HCl, H2O, heating
(c) Cumene, O2, H3O+
(d)
Ans: (d)
At STP condition substitution at sp2 carbon atom is not feasible.
Q2: Given below are two statements:
Statement I: The acidic strength of monosubstituted nitrophenol is higher than phenol because of the electron-withdrawing into the group.
Statement II: o-nitrophenol, m-nitrophenol, and p-nitrophenol will have same acidic strength as they have one nitro group attached to the phenolic ring.
In light of the above statements, choose the most appropriate answer from the options given below: (NEET 2022 Phase 1)
(a) Statement I is correct but Statement II is incorrect
(b) Statement I is incorrect but Statement II is correct
(c) Both Statement I and Statement II are correct
(d) Both Statement I and Statement II are incorrect
Ans: (a)
Statement I is correct, Statement II incorrect.
Q4: Given below are two statements:
Statement -I: In Lucas test, primary, secondary and tertiary alcohols are distinguished on the basis of their reactivity with conc. HCl + ZnCl2, known as Lucas Reagent.
Statement -II: Primary alcohols are most reactive and immediately produce turbidity at room temperature on reaction with Lucas Reagent.
In the light of the above statements, choose the most appropriate answer from the options given below: (NEET 2022 Phase 2)
(a) Statement I is correct but Statement II is incorrect
(b) Statement I is incorrect but Statement II is correct
(c) Both statement I and Statement II are correct
(d) Both Statement I and Statement II are incorrect
Ans: (a)
Primary, secondary and tertiary alcohols can be differentiated by their reaction with (HCl + anhy ZnCl2) Lucas reagent
Q1: Anisole on cleavage with HI gives : (NEET 2020)
(a)
(b)
(c)
(d)
Ans: (c)
Q1: The structure of intermediate A in the following reaction, is (NEET 2019)
(a)
(b)
(c)
(d)
Ans: B
Q1: In the reaction
the electrophile involved is (NEET 2018)
(a) dichloromethyl cation
(b) formyl cation
(c) dichloromethyl anion
(d) dichlorocarbene
Ans: (d)
Q2: The compound A on treatment with Na gives B, and with PCl5 gives C. B and C react together to give diethyl ether. A, B and C are in the order (NEET 2018)
(a) C2H5OH, C2H6, C2H5Cl
(b) C2H5OH, C2H5Cl, C2H5ONa
(c) C2H5Cl,C2H6,C2H5OH
(d) C2H5OH,C2H5ONa,C2H5Cl
Ans: (d)
Q3: Identify the major products P, Q and R in the following sequence of reaction: (NEET 2018)
(a)
(b)
(c)
(d)
Q1: The heating of phenylmethyl ethers with HI produces (NEET 2017)
(a) iodobenzene
(b) phenol
(c) benzene
(d) ethyl chlorides
Ans: (b)
In case of phenyl methyl ether, methyl phenyl oxonium ion
is formed by protonation of ether. The O—CH3 bond is weaker than O—C6H5 bond as O—C6H5 has partial double bond character. Therefore, the attack by I– ion breaks O—CH3 bond to form CH3I.
Q2: Which one is the most acidic compound? (NEET 2017)
(a)
(b)
(c)
(d)
Q1: The reaction:
can be classified as: (NEET 2016)
(a) Williamson alcohol synthesis reaction
(b) Williamson ether synthesis reaction
(c) Alcohol formation reaction
(d) Dehydration reaction
Q1: Reaction of phenol with chloroform in the presence of dilute sodium hydroxide finally introduces which one of the following functional groups? (NEET / AIPMT 2015)
(a) −COOH
(b) −CHCl2
(c) −CHO
(d) −CH2Cl
Ans: (c)
This is Reimer–Tiemann reaction.
Q2: Which of the following reaction(s) can be used for the preparation of alkyl halides? (NEET / AIPMT 2015)
(a) (I) and (II) only
(b) (IV) only
(c) (III) and (IV) only
(d) (I), (III), and (IV) only
Ans: (d)
Lucas reagent [HCl + ZnCl2] can be used for
1° / 2° / 3° alcohol but if ZnCl2 is absent then only 3° alcohol can be used because it is most reactive due to 3° carbocation.
Q3: The reaction
(AIPMT 2015 Cancelled Paper)
(a) Gatterman – Koch reaction
(b) Williamson Synthesis
(c) Williamson's continuous etherification process
(d) Etard reaction
Ans: (b)
The reaction is called Williamson synthesis
Q1: Which of the following will not be soluble sodium hydrogen carbonate? (NEET 2014)
(a) o−Nitrophenol
(b) Benzenesulphonic acid
(c) 2, 4, 6 − trinitrophenol
(d) Benzoic acid
Ans: (a)
Acid reacts with sodium hydrogen carbonate as follows :
Among all the given options ortho-nitrophenol is weaker acid than HCO3 hence, it does not react with NaHCO3.
108 videos|286 docs|123 tests
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1. What are the general properties of alcohols, phenols, and ethers ? |
2. How do the boiling points of alcohols compare to those of ethers and phenols ? |
3. What is the mechanism of the dehydration of alcohols to form alkenes ? |
4. What are the common methods for the synthesis of ethers ? |
5. What are the uses of alcohols, phenols, and ethers in daily life ? |
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