1
JEE Main 2025 (Online) 8th April Evening Shift
MCQ (Single Correct Answer)
+4
-1
Change Language

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, $$ { }^{\mathrm{t}} \mathrm{Bu} \Rightarrow \text { tert-butyl, } \mathrm{Et} \Rightarrow \text { ethyl) } $$

A
JEE Main 2025 (Online) 8th April Evening Shift Chemistry - Haloalkanes and Haloarenes Question 5 English Option 1
B
iso- $\mathrm{Bu} \overline{\mathrm{O}} \stackrel{+}{\mathrm{Na}}+\mathrm{sec}-\mathrm{BuBr} \longrightarrow$ sec- $\mathrm{Bu}-\mathrm{O}-$ iso -Bu
C
JEE Main 2025 (Online) 8th April Evening Shift Chemistry - Haloalkanes and Haloarenes Question 5 English Option 3
D
${ }^{\mathrm{t}}\mathrm{Bu}\overline{\mathrm{O}} \stackrel{+}{\mathrm{Na}}+\mathrm{EtBr} \longrightarrow{ }^{\mathrm{t}} \mathrm{Bu}-\mathrm{O}-\mathrm{Et}$
2
JEE Main 2025 (Online) 8th April Evening Shift
MCQ (Single Correct Answer)
+4
-1
Change Language

Match the LIST-I with LIST-II

LIST-I (Reagent)LIST-II (Functional Group detected)
A. Sodium bicarbonate solutionI. double bond/unsaturation
B. Neutral ferric chlorideII. carboxylic acid
C. ceric ammonium nitrateIII. phenolic - OH
D. alkaline KMnO4IV. alcoholic - OH

Choose the correct answer from the options given below:

A

A-II, B-III, C-I, D-IV

B

A-II, B-IV, C-III, D-I

C

A-III, B-II, C-IV, D-I

D

A-II, B-III, C-IV, D-I

3
JEE Main 2025 (Online) 8th April Evening Shift
MCQ (Single Correct Answer)
+4
-1
Change Language

JEE Main 2025 (Online) 8th April Evening Shift Chemistry - Aldehydes, Ketones and Carboxylic Acids Question 9 English

Choose the correct option for structures of $A$ and $B$, respectively

A
JEE Main 2025 (Online) 8th April Evening Shift Chemistry - Aldehydes, Ketones and Carboxylic Acids Question 9 English Option 1
B
JEE Main 2025 (Online) 8th April Evening Shift Chemistry - Aldehydes, Ketones and Carboxylic Acids Question 9 English Option 2
C
JEE Main 2025 (Online) 8th April Evening Shift Chemistry - Aldehydes, Ketones and Carboxylic Acids Question 9 English Option 3
D
JEE Main 2025 (Online) 8th April Evening Shift Chemistry - Aldehydes, Ketones and Carboxylic Acids Question 9 English Option 4
4
JEE Main 2025 (Online) 8th April Evening Shift
Numerical
+4
-1
Change Language

Consider the following half cell reaction

$$ \text{Cr}_2\text{O}_7^{2-} \, (\text{aq}) + 6\text{e}^- + 14\text{H}^+ \, (\text{aq}) \rightarrow 2\text{Cr}^{3+} \, (\text{aq}) + 7\text{H}_2\text{O} \, (\ell) $$

The reaction was conducted with the ratio of $$\frac{[\text{Cr}^{3+}]^2}{[\text{Cr}_2\text{O}_7^{2-}]} = 10^{-6}$$. The pH value at which the EMF of the half cell will become zero is __________.

(nearest integer value)

[Given: standard half cell reduction potential $$E^{\circ}_{\text{Cr}_2\text{O}_7^{2-}, \text{H}^+/\text{Cr}^{3+}} = 1.33\, \text{V}$$, $$\frac{2.303RT}{F} = 0.059\, \text{V}$$.]

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