JEE Mains
2026
MCQ
$\mathrm{Ph}-\mathrm{CH}=\mathrm{CH}_2 \xrightarrow[\mathrm{HBr}]{(\mathrm{PhCOO})_2}$ Product
Consider the above reaction
A. The reaction proceeds through a more stable radical intermediate.
B. The role of peroxide is to generate ${H^ \bullet }$ (Hydrogen radical).
C. During this reaction, benzene is formed as a byproduct.
D. 1-Bromo-2-phenylethane is formed as the minor product.
E. The same reaction in absence of peroxide proceeds via carbocation intermediate.
Identify the correct statements. Choose the correct answer from the options given below :
JEE Mains
2026
MCQ
Consider the following reactions giving major product. Identify the correct reaction.
JEE Mains
2026
MCQ
Given below are two statements :
Statement I : ' $\mathrm{C}-\mathrm{Cl}$ ' bond is stronger in $\mathrm{CH}_2=\mathrm{CH}-\mathrm{Cl}$ than $\mathrm{CH}_3-\mathrm{CH}_2-\mathrm{Cl}$
Statement II : The given optically active molecule,
on
hydrolysis gives a solution that can rotate the plane polarized light.
In the light of the above statements, choose the correct answer from the options given below
JEE Mains
2026
MCQ
Match the List-I with List-II
List-I Chloro derivative | List-II Example |
|---|
| A. Vinyl Chloride | I. CH$_2$ = CH - CH$_2$Cl |
| B. Benzyl Chloride | II. CH$_3$ - CH(Cl)CH$_3$ |
| C. Alkyl Chloride | III. CH$_2$ = CHCl |
| D. Allyl Chloride | IV.  |
Choose the correct answer from the options given below :
JEE Mains
2026
MCQ
$ \text { Consider the following compounds } $

$ \text { Arrange these compounds in the increasing order of reactivity with nitrating mixture. } $
JEE Mains
2026
MCQ
As compared with chlorocyclohexane, which of the following statements correctly apply to chlorobenzene?
A. The magnitude of negative charge is more on chlorine atom.
B. The $\mathrm{C}-\mathrm{Cl}$ bond has partial double bond character.
C. $\mathrm{C}-\mathrm{Cl}$ bond is less polar.
D. $\mathrm{C}-\mathrm{Cl}$ bond is longer due to repulsion between delocalised electrons of the aromatic ring and lone pairs of electrons of chlorine.
E. The $\mathrm{C}-\mathrm{Cl}$ bond is formed using $\mathrm{sp}^2$ hybridised orbital of carbon.
Choose the correct answer from the options given below :
JEE Mains
2026
MCQ
The correct order of the rate of reaction of the following reactants with nucleophile by $\mathrm{S}_{\mathrm{N}} 1$ mechanism is :
(Given : Structures I and II are rigid)
JEE Mains
2026
MCQ
The correct order of reactivity of $\mathrm{CH}_3 \mathrm{Br}$ in methanol with the following nucleophiles is
$\mathrm{F}^{-}, \mathrm{I}^{-}, \mathrm{C}_2 \mathrm{H}_5 \mathrm{O}^{-}$and $\mathrm{C}_6 \mathrm{H}_5 \mathrm{O}^{-}$
JEE Mains
2026
MCQ
The correct order of the rate of the reaction for the following reaction with respect to nucleophiles is :
${CH_3Br + Nu^- \longrightarrow CH_3Nu + Br^-}$
JEE Mains
2026
MCQ
The correct order of reactivity of the following benzyl halides towards reaction with KCN is :
JEE Mains
2026
MCQ
Given below are two statements :
Statement I : Due to increase in van der Waals forces, the order of boiling points is $\mathrm{CH}_3 \mathrm{CH}_2 \mathrm{CH}_2 \mathrm{I}>\mathrm{CH}_3 \mathrm{CH}_2 \mathrm{I}>\mathrm{CH}_3 \mathrm{I}$.
$ \text { Statement II : } $
In the light of the above statements, choose the correct answer from the options given below :
JEE Mains
2026
MCQ
Given below are two statements :
Statement I : 3-phenylpropene reacts with HBr and gives secondary alkyl bromide having a chiral carbon atom as the major product.
Statement II : Aryl chlorides and aryl cyanides can be prepared by Sandmeyer reaction as well as Gattermann reaction.
In the light of the above statements, choose the correct answer from the options given below
JEE Mains
2026
MCQ
$ \text { Match the LIST-I with LIST-II } $
$ \begin{gathered} \text { List-I } \\ \text { Name of reaction } \end{gathered} $
|
$ \begin{gathered} \text { List-II } \\ \text { Reagent or catalyst used } \end{gathered} $
|
| A. |
Finkelstein reaction |
I. |
$\mathrm{SbF}_3$ |
| B. |
Swarts reaction |
II. |
Na, dry ether |
| C. |
Sandmeyer's reaction |
III. |
NaI |
| D. |
Fittig reaction |
IV. |
$\mathrm{Cu}_2 \mathrm{Cl}_2$ |
Choose the correct answer from the options given below :
JEE Mains
2026
MCQ
Correct statements regarding alkyl halides (R–X) among the following are :
A. Alcohol being less polar solvent as compared to water, alcoholic KOH favours elimination reaction with R–X.
B. Order of reactivity towards SN1 mechanism is C6H5–CH2–Cl > C6H5–CHCl–C6H5.
C. Non substituted aryl halides exhibit properties similar to alkyl halides.
D. Vinyl chloride is an example of haloalkene and allyl chloride is an example of haloalkyne.
E. R–Cl can be prepared by reacting R–OH with SOCl2 but Ar–Cl cannot be prepared by reacting Ar–OH with SOCl2.
Choose the correct answer from the options given below :
JEE Mains
2026
MCQ
Given below are two statements :
Statement (I) : Benzyl chloride reacts faster in $S_N1$ mechanism than ethyl chloride.
Statement (II) : Ethyl carbocation intermediate is less stabilized by hyperconjugation than benzyl carbocation by resonance.
In the light of the above statements, choose the correct answer from the options given below :
JEE Mains
2025
MCQ

'P' is
JEE Mains
2025
MCQ
Choose the correct set of reagents for the following conversion.
JEE Mains
2025
MCQ
Which one of the following reactions will not lead to the desired ether formation in major proportion?
(iso- $\mathrm{Bu} \Rightarrow$ isobutyl, sec $-\mathrm{Bu} \Rightarrow$ sec-butyl, $\mathrm{nPr} \Rightarrow \mathrm{n}$-propyl, $ { }^{\mathrm{t}} \mathrm{Bu} \Rightarrow \text { tert-butyl, } \mathrm{Et} \Rightarrow \text { ethyl) } $
JEE Mains
2025
MCQ
Consider the following molecule(X).

The major product formed when the given molecule $(X)$ is treated with $\mathrm{HBr}(1 \mathrm{eq})$ is :
JEE Mains
2025
MCQ
Given below are two statements :
Statement (I) : Alcohols are formed when alkyl chlorides are treated with aqueous potassium hydroxide by elimination reaction.
Statement (II) : In alcoholic potassium hydroxide, alkyl chlorides form alkenes by abstracting the hydrogen from the $\beta$-carbon.
In the light of the above statements, choose the most appropriate answer from the options given below :
JEE Mains
2025
MCQ
$ \text {In the following series of reactions identify the major products } \mathrm{A} \& \mathrm{~B} \text { respectively } $
JEE Mains
2025
MCQ
Which among the following halides will generate the most stable carbocation in the nucleophilic substitution reaction?
JEE Mains
2025
MCQ
The major product of the following reaction is:
JEE Mains
2025
MCQ
The products A and B in the following reactions, respectively are
$\mathrm{A} \stackrel{\mathrm{Ag}-\mathrm{NO}_2}{\longleftrightarrow} \mathrm{CH}_3-\mathrm{CH}_2-\mathrm{CH}_2-\mathrm{Br} \xrightarrow{\mathrm{AgCN}} \mathrm{B}$
JEE Mains
2025
MCQ
The structure of the major product formed in the following reaction is :

JEE Mains
2025
MCQ
Given below are two statements:
Statement I: The conversion proceeds well in the less polar medium.
$\mathrm{CH}_3-\mathrm{CH}_2-\mathrm{CH}_2-\mathrm{CH}_2-\mathrm{Cl} \xrightarrow{\mathrm{HO}^{-}} \mathrm{CH}_3-\mathrm{CH}_2-\mathrm{CH}_2-\mathrm{CH}_2-\mathrm{OH}+\mathrm{Cl}^{(-)}$
Statement II: The conversion proceeds well in the more polar medium.

In the light of the above statements, choose the correct answer from the options given below
JEE Mains
2025
MCQ
Following are the four molecules "P", "Q", "R" and "S".
Which one among the four molecules will react with $\mathrm{H}-\mathrm{Br}_{(\mathrm{aq})}$ at the fastest rate?

JEE Mains
2025
MCQ
Identify the products [A] and [B], respectively in the following reaction:

JEE Mains
2025
MCQ
The ascending order of relative rate of solvolysis of following compounds is :

JEE Mains
2025
MCQ
Propane molecule on chlorination under photochemical condition gives two di-chloro products, " $x$ " and " $y$ ". Amongst " $x$ " and " $y$ ", " $x$ " is an optically active molecule. How many tri-chloro products (consider only structural isomers) will be obtained from " x " when it is further treated with chlorine under the photochemical condition?
JEE Mains
2025
MCQ

The maximum number of RBr producing 2-methylbutane by above sequence of reactions is
__________ . (Consider the structural isomers only)
JEE Mains
2025
MCQ
Given below are two statements :
Statement I : $\quad \mathrm{CH}_3-\mathrm{O}-\mathrm{CH}_2-\mathrm{Cl}$ will undergo $\mathrm{S}_{\mathrm{N}} 1$ reaction though it is a primary halide.
Statement II :
will not undergo $\mathrm{S}_{\mathrm{N}} 2$ reaction very easily though it is a primary halide.
In the light of the above statements, choose the most appropriate answer from the options given below :
JEE Mains
2024
MCQ
Given below are two statements : one is labelled as Assertion (A) and the other is labelled as Reason (R).
Assertion (A) : $\mathrm{S}_{\mathrm{N}} 2$ reaction of $\mathrm{C}_6 \mathrm{H}_5 \mathrm{CH}_2 \mathrm{Br}$ occurs more readily than the $\mathrm{S}_{\mathrm{N}} 2$ reaction of $\mathrm{CH}_3 \mathrm{CH}_2 \mathrm{Br}$.
Reason (R) : The partially bonded unhybridized p-orbital that develops in the trigonal bipyramidal transition state is stabilized by conjugation with the phenyl ring.
In the light of the above statements, choose the most appropriate answer from the options given below :
JEE Mains
2024
MCQ
In the following sequence of reaction, the major products B and C respectively are :

JEE Mains
2024
MCQ
Which among the following compounds will undergo fastest SN2 reaction.
JEE Mains
2024
MCQ
Identify the major product in the following reaction.

JEE Mains
2024
MCQ

Product P is
JEE Mains
2024
MCQ
$\mathrm{CH}_3-\mathrm{CH}_2-\mathrm{CH}_2-\mathrm{Br}+\mathrm{NaOH} \xrightarrow{\mathrm{C}_2 \mathrm{H}_5 \mathrm{OH}} \text { Product 'A' }$

Consider the above reactions, identify product B and product C.
JEE Mains
2024
MCQ
Find out the major product formed from the following reaction. $[\mathrm{Me}:-\mathrm{CH}_3]$

JEE Mains
2024
MCQ

Identify B and C and how are A and C related?
JEE Mains
2024
MCQ
Identify the correct set of reagents or reaction conditions '$X$' and '$Y$' in the following set of transformation.

JEE Mains
2024
MCQ
Given below are two statements : one is labelled as Assertion (A) and the other is labelled as Reason (R).
Assertion (A) : Haloalkanes react with KCN to form alkyl cyanides as a main product while with $\mathrm{AgCN}$ form isocyanide as the main product.
Reason (R) : $\mathrm{KCN}$ and $\mathrm{AgCN}$ both are highly ionic compounds.
In the light of the above statements, choose the most appropriate answer from the options given below :
JEE Mains
2024
MCQ
Identify A and B in the following reaction sequence.

JEE Mains
2024
MCQ
The product (C) in the below mentioned reaction is :
$\mathrm{CH}_3-\mathrm{CH}_2-\mathrm{CH}_2-\mathrm{Br} \xrightarrow[\Delta]{\mathrm{KOH}_{(\text {alc) }}} \mathrm{A} \xrightarrow{\mathrm{HBr}} \mathrm{B} \xrightarrow[\mathrm{KOH}_{(\mathrm{aq})}]{\Delta} \mathrm{C}$
JEE Mains
2024
MCQ
Given below are two statements:
Statement - I: High concentration of strong nucleophilic reagent with secondary alkyl halides which do not have bulky substituents will follow $\mathrm{S}_{\mathrm{N}}{ }^2$ mechanism.
Statement - II: A secondary alkyl halide when treated with a large excess of ethanol follows $\mathrm{S}_{\mathrm{N}}{ }^1$ mechanism.
In the light of the above statements, choose the most appropriate from the options given below:
JEE Mains
2024
MCQ
Example of vinylic halide is :
JEE Mains
2024
MCQ
The final product A, formed in the following multistep reaction sequence is :

JEE Mains
2024
MCQ
Given below are two statements : one is labelled as Assertion (A) and the other is labelled as Reason (R).
Assertion (A) : $\mathrm{CH}_2=\mathrm{CH}-\mathrm{CH}_2-\mathrm{Cl}$ is an example of allyl halide.
Reason (R) : Allyl halides are the compounds in which the halogen atom is attached to $\mathrm{sp}^2$ hybridised carbon atom.
In the light of the above statements, choose the most appropriate answer from the options given below :
JEE Mains
2024
MCQ
Alkyl halide is converted into alkyl isocyanide by reaction with
JEE Mains
2024
MCQ
Given below are two statements : one is labelled as Assertion A and the other is labelled as Reason R :
Assertion A : Aryl halides cannot be prepared by replacement of hydroxyl group of phenol by halogen atom.
Reason R : Phenols react with halogen acids violently.
In the light of the above statements, choose the most appropriate from the options given below :
JEE Mains
2024
MCQ
Identify B formed in the reaction.
$\mathrm{Cl}-\left(\mathrm{CH}_2\right)_4-\mathrm{Cl} \xrightarrow{\text { excess } \mathrm{NH}_3} \mathrm{~A} \xrightarrow{\mathrm{NaOH}} \mathrm{B}+\mathrm{H}_2 \mathrm{O}+\mathrm{NaCl}$
JEE Mains
2024
MCQ
Which among the following halide/s will not show $\mathrm{S_N 1}$ reaction:
(A) $\mathrm{H}_2 \mathrm{C}=\mathrm{CH}-\mathrm{CH}_2 \mathrm{Cl}$
(B) $\mathrm{CH}_3-\mathrm{CH}=\mathrm{CH}-\mathrm{Cl}$
(C) 
(D) 
Choose the most appropriate answer from the options given below :
JEE Mains
2024
MCQ
The correct statement regarding nucleophilic substitution reaction in a chiral alkyl halide is ;
JEE Mains
2023
MCQ
The major product formed in the Friedel-Craft acylation of chlorobenzene is
JEE Mains
2023
MCQ
In the following reaction 'X' is

JEE Mains
2023
MCQ
Compound from the following that will not produce precipitate on reaction with $\mathrm{AgNO}_{3}$ is :
JEE Mains
2023
MCQ

Find out the correct statement from the options given below for the above 2 reactions.
JEE Mains
2023
MCQ
Identify the correct order of reactivity for the following pairs towards the respective mechanism

Choose the correct answer from the options given below:
JEE Mains
2023
MCQ
The pair from the following pairs having both compounds with net non-zero dipole moment is
JEE Mains
2023
MCQ
Major product '$\mathrm{P}$' formed in the following reaction is:

JEE Mains
2023
MCQ
The correct order of reactivity of following haloarenes towards nucleophilic substitution with aqueous $\mathrm{NaOH}$ is :

Choose the correct answer from the options given below:
JEE Mains
2023
MCQ
Choose the halogen which is most reactive towards $\mathrm{S}_{\mathrm{N}} 1$ reaction in the given compounds (A, B, C & D)

JEE Mains
2023
MCQ
For the reaction

The correct statement is
JEE Mains
2023
MCQ
In the following halogenated organic compounds, the one with the maximum number of chlorine atoms in its structure is :
JEE Mains
2023
MCQ
The correct order of melting points of dichlorobenzenes is
JEE Mains
2023
MCQ
Decreasing order towards SN 1 reaction for the following compounds is:

JEE Mains
2023
MCQ
Match List I with List II
|
List I |
|
List II |
| A. |
 |
I. |
Fittig reaction |
| B. |
 |
II. |
Wurtz Fittig reaction |
| C. |
 |
III. |
Finkelstein reaction |
| D. |
$\mathrm{C_5H_5C1+NaI\to C_2H_5I+NaCl}$ |
IV. |
Sandemyer reaction |
Choose the correct answer from the options given below :
JEE Mains
2023
MCQ
Identify the correct order for the given property for following compounds.

Choose the correct answer from the option given below :
JEE Mains
2023
MCQ
The isomeric deuterated bromide with molecular formula $\mathrm{C_4H_8DBr}$ having two chiral carbon atoms is
JEE Mains
2023
MCQ
The compound which will have the lowest rate towards nucleophilic aromatic substitution on treatment with OH$^-$ is
JEE Mains
2023
MCQ
Assertion A : Hydrolysis of an alkyl chloride is a slow reaction but in the presence of NaI, the rate of the hydrolysis increases.
Reason R : I$^{-}$ is a good nucleophile as well as a good leaving group.
In the light of the above statements, choose the correct answer from the options given below
JEE Mains
2022
MCQ
Compound 'A' undergoes following sequence of reactions to give compound 'B'.
The correct structure and chirality of compound 'B' is
[where Et is $\left.-\mathrm{C}_{2} \mathrm{H}_{5}\right]$

JEE Mains
2022
MCQ
Which among the following pairs of the structures will give different products on ozonolysis? (Consider the double bonds in the structures are rigid and not delocalized.)
JEE Mains
2022
MCQ

Considering the above reactions, the compound 'A' and compound 'B' respectively are :
JEE Mains
2022
MCQ
The major product in the given reaction is

JEE Mains
2022
MCQ
Major product '$\mathrm{B}$' of the following reaction sequence is :

JEE Mains
2022
MCQ

The stable carbocation formed in the above reaction is
JEE Mains
2022
MCQ
Two isomers (A) and (B) with Molar mass 184 g/mol and elemental composition C, 52.2%; H, 4.9% and Br 42.9% gave benzoic acid and p-bromobenzoic acid, respectively on oxidation with KMnO4. Isomer 'A' is optically active and gives a pale yellow precipitate when warmed with alcoholic AgNO3. Isomer 'A' and 'B' are, respectively
JEE Mains
2022
MCQ

In the given conversion the compound A is :
JEE Mains
2022
MCQ
In the above reaction 'A' is
JEE Mains
2022
MCQ
The major product (P) in the reaction

is
JEE Mains
2022
MCQ
Which one of the following compounds is inactive towards SN1 reaction?
JEE Mains
2022
MCQ
The major product of the following reaction is :
JEE Mains
2022
MCQ
Halogenation of which one of the following will yield m-substituted product with respect to methyl group as a major product?
JEE Mains
2022
MCQ
The major product in the reaction

JEE Mains
2022
MCQ
In the given reaction sequence, the major product 'C' is :

JEE Mains
2021
MCQ
In the following sequence of reactions,

The compounds B and C respectively are :-
JEE Mains
2021
MCQ
The major product of the following reaction is :
JEE Mains
2021
MCQ
The correct order of reactivity of the given chlorides with acetate in acetic acid is :
JEE Mains
2021
MCQ
The major product (A) formed in the reaction given below is :
JEE Mains
2021
MCQ
In the following sequence of reactions the P is :
JEE Mains
2021
MCQ

Consider the given reaction, the product A is :
JEE Mains
2021
MCQ
The major product formed in the following reaction is :
JEE Mains
2021
MCQ
Among the following compounds I-IV, which one forms a yellow precipitate on reacting sequentially with (i) NaOH (ii) dil. HNO
3 (iii) AgNO
3?
JEE Mains
2021
MCQ
Excess of isobutane on reaction with Br2 in presence of light at 125$^\circ$C gives which one of the following, as the major product?
JEE Mains
2021
MCQ

The given reaction can occur in the presence of :
(a) Bromine water
(b) Br
2 in CS
2, 273 K
(c) Br
2/FeBr
3(d) Br
2 in CHCl
3, 273 K
Choose the correct answer from the options gien below :
JEE Mains
2021
MCQ
Given below are two statements :
Statement I : C2H5OH and AgCN both can generate nucleophile.
Statement II : KCN and AgCN both will generate nitrile nucleophile with all reaction conditions.
Choose the most appropriate option :
JEE Mains
2021
MCQ
Main products formed during a reaction of 1-methoxy naphthalene with hydroiodic acid are :
JEE Mains
2021
MCQ
Reaction of Grignard reagent, C2H5MgBr with C8H8O followed by hydrolysis gives compound "A" which reacts instantly with Lucas reagent to give compound B, C10H13Cl. The Compound B is :
JEE Mains
2021
MCQ
The correct pair(s) of the ambident nucleophiles is(are)
(A) AgCN/KCN
(B) RCOOAg/RCOOK
(C) AgNO2/KNO2
(D) AgI/KI
JEE Mains
2021
MCQ

The above reaction requires which of the following reaction conditions?
JEE Mains
2021
MCQ

Product ''A'' in the above chemical reaction is :
JEE Mains
2021
MCQ
Which of the following reaction is an example of ammonolysis?
JEE Mains
2021
MCQ

Identify the reagent(s) 'A' and condition(s) for the reaction
JEE Mains
2021
MCQ

The products ''A'' and ''B'' formed in above reactions are :
JEE Mains
2021
MCQ
Match List - I with List - II.

Choose the correct answer from the options given below :
JEE Mains
2021
MCQ
For the given reaction

What is 'A'?
JEE Mains
2021
MCQ
For the given reaction :

What is 'A'?
JEE Mains
2021
MCQ
Identify A and B in the chemical reaction.
JEE Mains
2021
MCQ
What is the major product formed by HI on reaction with
JEE Mains
2021
MCQ
The product formed in the first step of the reaction of

with excess $\mathrm{Mg/Et_2O}$ ($\mathrm{Et=C_2H_5}$) is
JEE Mains
2020
MCQ
The increasing order of the boiling points of
the major products A, B and C of the following
reactions will be :
JEE Mains
2020
MCQ
The major product formed in the following reaction is :
CH3CH = CHCH(CH3)2 $\buildrel {HBr} \over
\longrightarrow $
JEE Mains
2020
MCQ
Among the following compounds, which one
has the shortest C – Cl bond?
JEE Mains
2020
MCQ
Which of the following compounds will form the
precipitate with aq. AgNO3 solution most
readily?
JEE Mains
2020
MCQ
The decreasing order of reactivity of the
following organic molecules towards AgNO
3
solution is :
JEE Mains
2020
MCQ
The decreasing order of reactivity of the
following compounds towards nucleophilic
substitution (S
N2) is :
JEE Mains
2020
MCQ
The major product in the following reaction is :
JEE Mains
2020
MCQ
The mechanism of S
N1 reaction is given as :
A student writes general characteristics based
on the given mechanism as :
(a) The reaction is favoured by weak
nucleophiles.
(b) R
+ would be easily formed if the
substituents are bulky.
(c) The reaction is accompanied by
racemization.
(d) The reaction is favoured by non-polar
solvents.
JEE Mains
2020
MCQ
The major product obtained from
E2 - elimination of 3-bromo-2-fluoropentane is
JEE Mains
2020
MCQ
Consider the reaction sequence given below:
Which of the following statements is true?
JEE Mains
2020
MCQ
Which of the following compunds will show
retention in configuration on nucleophilic
substitution by OH– ion?
JEE Mains
2020
MCQ
Which of the following reactions will not
produce a racemic product?
JEE Mains
2020
MCQ
Which of these will produce the highest yield
in Friedel Crafts reaction?
JEE Mains
2020
MCQ
The decreasing order of reactivity towards dehydrohalogenation (E
1) reaction of the following compounds is :
JEE Mains
2020
MCQ
For the following reactions

K
s and K
e, are respectively, the rate constants for substitution and elimination and $\mu = {{{k_s}} \over {{k_e}}}$ the
correct options is
JEE Mains
2020
MCQ
1- methyl ethylene oxide when treated with an excess of HBr produces :
JEE Mains
2019
MCQ
Which one of the following is likely to give a precipitate with AgNO3 solution ?
JEE Mains
2019
MCQ
An 'Assertion' and a 'Reason' are given below. Choose the correct answer from the following options :
Assertion (A) : Vinyl halides do not undergo nucleophilic substitution easily.
Reason (R) : Even though the intermediate carbocation is stabilized by loosely held p-electrons, the cleavage
is difficult because of strong bonding.
JEE Mains
2019
MCQ
Heating of 2-chloro-1-phenylbutane with EtOK/EtOH gives X as the major product. Reaction of X with
Hg(OAc)2/H2O followed by NaBH4 gives Y as the major product. Y is :
JEE Mains
2019
MCQ
The major product 'Y' in the following reactions is :
JEE Mains
2019
MCQ
The major product obtained in the given reaction is :
JEE Mains
2019
MCQ
Increasing rate of S
N1 reaction in the following compounds is :
JEE Mains
2019
MCQ
The major product of the following reaction is :
JEE Mains
2019
MCQ
Which one of the following alkenes when
treated with HCl yields majorly an anti
Markovnikov product?
JEE Mains
2019
MCQ
The major product in the following reaction is :
JEE Mains
2019
MCQ
The major product of the following reaction is:
JEE Mains
2019
MCQ
The major product in the following conversion is –
JEE Mains
2019
MCQ
Which of the following compounds will produce a precipitate with AgNO3 ?
JEE Mains
2019
MCQ
Which hydrogen in compound (E) is easily replaceable during bromination reaction in presence of light ?
JEE Mains
2019
MCQ
The major product of the following reaction is :
JEE Mains
2019
MCQ
The compounds A and B in the following reaction are, respectively :
JEE Mains
2019
MCQ
The major product of the following reaction is :
JEE Mains
2018
MCQ
The most polar compound among the following is :
JEE Mains
2018
MCQ
The major product of the following reaction is :
JEE Mains
2018
MCQ
The major product of the following reaction is:
JEE Mains
2017
MCQ
In the following reaction sequence :
The compound I is :
JEE Mains
2017
MCQ
The major product of the following reaction is :
JEE Mains
2017
MCQ
The major product of the following reaction is :
JEE Mains
2017
MCQ
Which of the following compounds will not undergo Friedel Craft’s reaction with benzene ?
JEE Mains
2017
MCQ
Which of the following, upon treatment with tert-BuONa followed by addition of bromine water, fails to
decolorize the colour of bromine?
JEE Mains
2017
MCQ
3-Methyl-pent-2-ene on reaction with HBr in presence of peroxide forms an addition product. The number
of possible stereoisomers for the product is :
JEE Mains
2017
MCQ
The increasing order of the reactivity of the following halides for the S
N1 reaction is :
JEE Mains
2017
MCQ
The major product obtained in the following reaction is :
JEE Mains
2016
MCQ
Bromination of cyclohexene under conditions given below yields :
JEE Mains
2016
MCQ
Which one of the following reagents is not suitable for the elimination reaction ?
JEE Mains
2015
MCQ
The synthesis of alkyl fluorides is best accomplished by:
JEE Mains
2014
MCQ
In SN2 reactions, the correct order of reactivity for the following compounds:
CH3Cl, CH3CH
2Cl, (CH3)2CHCl and (CH3)3CCl is:
JEE Mains
2014
MCQ
The major organic compound formed by the reaction of 1, 1, 1– trichloroethane with silver powder is:
JEE Mains
2013
MCQ
A solution of (–$l$) – chloro –1 – phenylethane in toluene racemises slowly in the presence of a small
amount of SbCl5, due to the formation of :
JEE Mains
2013
MCQ
Compound $\left( A \right),\,{C_8}{H_9}Br,\,\,\,$ gives a white precipitate when warmed with alcoholic $AgN{O_3}.$ Oxidation of $(A)$ gives an acid $\left( B \right),$ ${C_8}{H_6}{O_4}.\,\,\left( B \right)$ easily forms anhydride on heating. Identify the compound $(A).$
JEE Mains
2012
MCQ
What is DDT among the following?
JEE Mains
2012
MCQ
Iodoform can be prepared from all except :
JEE Mains
2012
MCQ
How many chiral compounds are possible on monochlorination of 2–methyl butane ?
JEE Mains
2010
MCQ
Consider the following bromides :
The correct order of ${S_N}1$ reactive is
JEE Mains
2009
MCQ
Which of the following on heating with aqueous KOH, produces acetaldehyde ?
JEE Mains
2008
MCQ
The organic chloro compound, which shows complete stereochemical inversion during a SN2 reaction,
is
JEE Mains
2007
MCQ
Which of the following is the correct order of decreasing SN2 reactivity?
JEE Mains
2006
MCQ
The structure of the major product formed in the following reaction
is
JEE Mains
2006
MCQ
Fluorobenzene (C6H5F) can be synthesized in the laboratory
JEE Mains
2006
MCQ
Reaction of trans-2-phenyl-1-bromocyclopentane on reaction with alcoholic KOH produces
JEE Mains
2005
MCQ
Alkyl halides react with dialkyl copper reagents to give
JEE Mains
2005
MCQ
Elimination of bromine from 2-bromobutane results in the formation of-
JEE Mains
2005
MCQ
Tertiary alkyl halides are practically inert to substitution by SN2 mechanism because of
JEE Mains
2004
MCQ
The compound formed on heating chlorobenzene with chloral in the presence concentrated
sulphuric acid is
JEE Mains
2003
MCQ
Bottles containing C6H5l and C6H5CH2I lost their original labels. They were labelled A and B for testing A and B were separately taken in test tubes and boiled with NaOH solution. The end solution in each tube was made acidic with dilute HNO3 and then some AgNO3 solution was added. Substance B gave a yellow precipitate. Which one of the following statements is true for this experiment?
JEE Mains
2002
MCQ
The reaction :
${(CH)_3}C - Br\buildrel {{H_2}O} \over
\longrightarrow {(CH)_3}C - OH$