Question
Read the passage given below and answer the following questions: A compound (X) containing C, H and O is unreactive towards sodium. It also does not react with Schiff s reagent. On refluxing with an excess of hydroiodic acid, (X) yields only one organic product ( Y). On hydrolysis, (Y) yields a new compound (Z) which can be converted into (Y) by reaction with red phosphorus and iodine. The compound (Z) on oxidation with potassium permanganate gives a carboxylic acid. The equivalent weight of this acid is 60. The following questions are multiple choice questions. Choose the most appropriate answer:
  1. The compound (X) is an:
  1. Acid.
  2. Aldehyde.
  3. Alcohol.
  4. Ether.
  1. The IUPAC name of the acid formed is:
  1. Methanoic acid.
  2. Ethanoic acid.
  3. Propanoic acid.
  4. Butanoic acid.
  1. Compound (Y) is:
  1. Ethyl iodide.
  2. Methyl iodide.
  3. Propyl iodide.
  4. Mixture of (a) and (b).
  1. Compound (Z) is:
  1. Methanol.
  2. Ethanol.
  3. Propanol.
  4. Butanol.
  1. Compound (X) on treatment with excess of $Cl_2$ in presence of tight gives:
  1. $\propto-$ Chlorodiethyl ether.
  2. $\propto,\propto'-$ Dichlorodiethyl ether.
  3. Perchlorodiethyl ether.
  4. None of these.

Answer

  1. (d) Ether.
Explanation:
Since the compound X is unreactive towards sodium so it is neither an acid nor an alcohol. Since the compound X is unreactive towards Schiff's base so it is not an aldehyde.
The compound X forms only one product on reaction with excess HI, indicates that the compound X may be ether.
  1. (b) Ethanoic acid.
Explanation:
The reactions can be written as:

Since the equivalent weight of carboxylic acid is 60. So, it must be $CH_3COOH$ i.e., ethanoic acid.
  1. (a) Ethyl iodide.
​​​​​​​​​​​​​​​​​​​​​Explanation:
The alcohol Z in that case should be $C_2H_5OH$ and the compound Y should be ethyl iodide. X is therefore diethyl ether $(C_2H_5 — O — C_2H_5)​​​​​​​$
  1. (b) Ethanol.
  2. (c) Perchlorodiethyl ether.
​​​​​​​​​​​​​​​​​​​​​​​​​​​​Explanation:
In the presence of light and excess of chlorine, all the hydrogen atoms of diethyl ether are substituted to give perchlorodiethyl ether.
$\text{CH}_3\text{CH}_2-\text{O}-\text{CH}_2\text{CH}_3+10\text{Cl}_2\xrightarrow{\text{hu}}\\ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \text{(excess)}$
$\text{CCl}_3\text{CC}_2-\text{O}-\text{CCl}_2-\text{CCl}_3+\text{10HCI}\\ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \text{Perchlorodierhyl ether }$​​​​​​​

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  1. A
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  1.  
  1.  
  1.  
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Molar conductivity of ions are given as product of charge on ions to their ionic mobilities and Faradays constant.
$\lambda_\text{A}\text{n}+=\text{n}\mu_\text{A}\text{n}+\text{F}$ (here $\mu$ is the ionic mobility of $A^{n+})$
For electrolytes say $A_xB_y,$ molar conductivity is given by
$\lambda_{\text{m}(\text{A}_\text{x}\text{B}_\text{y})}=\text{x}_\text{n}\mu_{\text{A}^\text{n}}+\text{F}+\text{y}_\text{m}\lambda_{\text{A}^\text{m}}-\text{F}$
Ions
Ionic mobility
$K^+$
$7.616 \times 10^{-4}$
$Ca^{2+}$
$12.33 \times 10^{-4}$
$Br^-$
$8.09 \times 10^{-4}$
$\text{SO}_{4}^{2-}$
$16.58 \times 10^{-4}$
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  1. $256 \times 10^{-4}$
  2. $279$
  3. $23.7$
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  1. $LiCl = NaCl = KCl$
  2. $LiCl > NaCl > KCl$
  3. $KCl > LiCl > NaCl$
  4. $KCl > NaCl > LiCl$
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  1. $ohm^{-1}\ cm^2\ eq^{-1}$
  2. $ohm\ cm^2\ eq-1$
  3. $ohm^{-1}\ cm\ eq^{-1}$
  4. $ohm\ cm^{-2}\ eq^{-2}$
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  1. $120.18 \times 10^{-4}$
  2. $135 \times 10^{-4}$
  3. $273.54 \times 10^{-4}$
  4. $192.1 \times 10^{-4}$