- A. increases about three times
- B. increases about six times
- C. increases about ten times
- D. remains same
The depression in freezing point ($\Delta T_f$) is a colligative property given by $\Delta T_f = i \cdot K_f \cdot m$. For glucose, which is a non-electrolyte, the van't Hoff factor $i = 1$. For $MgCl_2$, which is an electrolyte, it dissociates as $MgCl_2 \rightarrow Mg^{2+} + 2Cl^-$, giving $i = 3$. Since the molality ($m$) is the same for both, $\Delta T_f$ for $MgCl_2$ will be approximately 3 times that of glucose.
- A. $H_2$ only
- B. Na metal only
- C. Na and $Cl_2$
- D. $H_2, Cl_2$ and NaOH
During the electrolysis of aqueous $NaCl$ (brine), water is reduced at the cathode to form $H_2$ gas and $OH^-$ ions. Chloride ions are oxidized at the anode to form $Cl_2$ gas. The remaining $Na^+$ and $OH^-$ ions in the solution form $NaOH$. Thus, the products are $H_2$, $Cl_2$, and $NaOH$.
- A. zero order kinetics
- B. first order kinetics
- C. second order kinetics
- D. third order kinetics
Radioactive decay is a spontaneous process where the rate of disintegration is directly proportional to the number of radioactive nuclei present at that time. This follows first-order kinetics, described by the rate law $Rate = -dN/dt = \lambda N$.
- A. Kinetic energy
- B. Potential energy
- C. Activation energy
- D. Collision frequency
Activation energy ($E_a$) is defined as the minimum extra amount of energy absorbed by a reactant system to reach the threshold energy level, which is required for the formation of the activated complex during a chemical reaction.
- A. $KMnO_4$ oxidises iodide ion to iodine in acid medium
- B. Permanganate is diamagnetic
- C. Copper liberates hydrogen from acids
- D. $Ti^{2+}$ liberates hydrogen from dilute acids
Copper ($Cu$) has a positive reduction potential ($E^\circ_{Cu^{2+}/Cu} = +0.34V$), meaning it is a weaker reducing agent than hydrogen. Therefore, it cannot displace hydrogen from dilute acids. The other options are correct: $KMnO_4$ is a strong oxidizer, $MnO_4^-$ is diamagnetic ($d^0$ configuration), and $Ti^{2+}$ is a strong reducing agent.
- A. $[Fe(CO)_5]$
- B. $[Fe(CN)_6]^{3-}$
- C. $[Fe(H_2O)_6]^{3+}$
- D. $[Fe(C_2O_4)_3]^{3-}$
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Log in to view solution →- A. A – i, B – ii, C – iii, D – iv
- B. A – iv, B – iii, C – ii, D – i
- C. A – iv, B – ii, C – iii, D – i
- D. A – i, B – iii, C – ii, D – iv
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Log in to view solution →- A. cyanide
- B. isocyanide
- C. alkyl nitrite
- D. nitroalkane
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Log in to view solution →- A. chloroquine
- B. chloramphenicol
- C. halothane
- D. chloroform
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Log in to view solution →- A. $C_6H_5 – CH_2 – CH_2OH$
- B. $C_6H_5 – CH_2 – CH(CH_3) – OH$
- C. $C_6H_5 – CH_2 OH$
- D. $CH_3CH_2OH$
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Log in to view solution →- A. o – nitrophenol
- B. phenol
- C. p – nitrophenol
- D. ethanol
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Log in to view solution →- A. Zinc amalgam + conc. $HNO_3$
- B. Zinc amalgam + conc. HCl
- C. Sodium amalgam + conc. $HNO_3$
- D. Sodium amalgam + conc. HCl
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Log in to view solution →- A. $H_3PO_2 + H_2O$
- B. $SnCl_2 / HCl$
- C. $LiAlH_4$
- D. $H_3PO_4$
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Log in to view solution →- A. quaternary ammonium salt
- B. primary amine
- C. secondary amine
- D. tertiary amine
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Log in to view solution →- A. Statement – I and Statement – II are correct
- B. Statement – I and Statement – II are incorrect
- C. Statement – I is correct and Statement – II is incorrect
- D. Statement – I is incorrect and Statement – II is correct
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