Match the compounds in List-I with the appropriate observations in List-II and choose the correct option.
| List–I | List–II |
|---|---|
(P) ![]() |
(1) Reaction with phenyl diazonium salt gives yellow dye. |
(Q) ![]() |
(2) Reaction with ninhydrin gives purple color and it also reacts with FeCl3 to give violet color. |
(R) ![]() |
(3) Reaction with glucose will give corresponding hydrazone. |
(S) ![]() |
(4) Lassiagne extract of the compound treated with dilute HCl followed by addition of aqueous $\mathrm{FeCl}_3$ gives blood red color. |
| (5) After complete hydrolysis, it will give ninhydrin test and it DOES NOT give positive phthalein dye test. |
P → 1; Q → 5; R → 4; S → 2
P → 2; Q → 5; R → 1; S → 3
P → 5; Q → 2; R → 1; S → 4
P → 2; Q → 1; R → 5; S → 3
The mass (in mg) of $\mathbf{S}$ obtained is ________.
[Use molar mass (in $\mathrm{g} \mathrm{mol}^{-1}$ ) : $\mathrm{H}=1, \mathrm{C}=12, \mathrm{~N}=14, \mathrm{Br}=80$ ]
Explanation:
First, calculate the moles of 4-methyloct-1-ene. The molar mass of 4-methyloct-1-ene is 126 g/mol. So, the moles of 4-methyloct-1-ene are :
$n_{4-\text{methyloct-1-ene}} = \frac{2.52 \, g}{126 \, g/mol} = 0.02 \, mol$
Given that the combined yield is 50%, the amount of isomeric bromides produced will be half of the initial amount, which is 0.01 mol.
The isomeric bromides are produced in a 9 : 1 ratio, so 90% of the product, or 0.009 mol, is the primary alkyl bromide. This is the compound that reacts further with diethylamine.
The reaction with diethylamine leads to the non-ionic product S with 100% yield, so we will still have 0.009 mol of product S.
Based on the chemical structures provided, the molar mass of S is 199 g/mol.
We can now calculate the mass of product S using the equation :
$ \text{Mass of S} = \text{moles of S} \times \text{molar mass of S} = 0.009 \, mol \times 199 \, g/mol = 1.791 \, g$
To convert this into milligrams, we multiply by 1000, yielding a mass of S obtained equal to 1791 mg.
Consider the following reaction.

On estimation of bromine in $1.00 \mathrm{~g}$ of $\mathbf{R}$ using Carius method, the amount of $\mathrm{AgBr}$ formed (in $\mathrm{g}$ ) is ___________.
[Given: Atomic mass of $\mathrm{H}=1, \mathrm{C}=12, \mathrm{O}=16, \mathrm{P}=31, \mathrm{Br}=80, \mathrm{Ag}=108]$
Explanation:
$2P+3Br_2\to2PBr_3$

Number of moles in 1 gm of (R) = $\frac{1}{250}$
Number of moles of AgBr formed from (R) = $\frac{2}{250}$
Mass of AgBr formed $=\frac{2\times188}{250}=1.50$ gm
The weight percentage of hydrogen in $\mathbf{Q}$, formed in the following reaction sequence, is ________.

[Given: Atomic mass of $\mathrm{H}=1, \mathrm{C}=12, \mathrm{~N}=14, \mathrm{O}=16, \mathrm{~S}=32, \mathrm{Cl}=35$ ]
Explanation:

Formula of compound = C6H3N3O7
Molar Mass of compound = (12 $\times$ 6 + 3 + 14 $\times$ 3 + 16 $\times$ 7) g = 229 g
Weight % of H = $\frac{3}{229}\times100=1.31$




Amide ( $-\mathrm{CO}-\mathrm{NH}-$ ) bond is present. It is known as peptide bond It is a dipeptide.This gives ninhydrin test. The result is a purple color.Ninhydrin test is used to detect the presence of amines in a sample.The test works by reacting ninhydrin with the free amino group $\left(-\mathrm{NH}_2\right)$. The result of the test is a purple color.The above dipeptide react with ninhydrin, the alpha -amino group (present in the above structure) undergoes reaction to give purple color:The compound also reacts with $\mathrm{FeCl}_3$ to give violet color. It is due to the free - OH group. It is a characteristic reaction of phenols
So, The compound $P$ reaction with ninhydrin gives purple color and it also reacts with $\mathrm{FeCl}_3$ to give violet color.$
P-2
$
Ninhyduin test is possible with free $-\mathrm{NH}_2$ group.
The above dipeptide on hydrolysis gives two amino acid molecules. So, after hydrolysis, ninhydrin test is possible. Because amino acids have free, $\mathrm{NH}_2$ group.But the compound does not give phthalein dye test.Phthalein dye test - It is used to identify the presence of phenolic functional groups. The compound has no free -OH group and hence it does not give phthalein dye test. For phthalein dye test, $-O H$ group must be attached directly to the momatic ring. So, The compound Q after complete hydrolysis give ninhydrin test and it does not give positive phthalein dye test.$
Q-5
$
$
\text { Aniline hydrochboide. (Aniline + HCI) }
$Aniline hydrochloride reacts with phenyl diazonium salt (benzene diazonium salt) and forms a dye ( $p$-aminoarobenzene) with yellow color.
So, compound $R$ reaction with phenyl diazonium salt gives yellow dye.$
R-1
$
It is a hydrazine. It reacts with glucose and give corresponding hydrazone.$
\text { It can be simply written as. }
$
So, S reaction with glucose give corresponding hydrazone.$S-3$$
\begin{aligned}
&\text { Answer: Option (B) }\\
&P \rightarrow 2, Q \rightarrow 5, R \rightarrow 1, S \rightarrow 3
\end{aligned}
$