Electrochemistry — NEET UG practice

73 questions

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Sample questions with solutions

Q1 · 2026

For a salt XY, which is a strong electrolyte, the plot of Λm\Lambda_{\mathrm{m}} versus c\sqrt{\mathrm{c}} has a slope of 90.0 S cm2 mol3/2L1/2-90.0 \mathrm{~S} \mathrm{~cm}^2 \mathrm{~mol}^{-3 / 2} \mathrm{L}^{1 / 2} at 298 K . At 0.01 M concentration of XY\mathbf{X Y}, the value of Λm\Lambda_{\mathrm{m}} is 145.0 S cm2 mol1145.0 \mathrm{~S} \mathrm{~cm}^2 \mathrm{~mol}^{-1}. The limiting molar conductivity of Y\mathbf{Y}^{-}ion (λY0\left(\lambda_{\mathbf{Y}^{-}}^0\right., in Scm2 mol1)\left.\mathrm{S} \mathrm{cm}^2 \mathrm{~mol}^{-1}\right) at 298 K will be (Given : λX+0=74.0 S cm2 mol1\lambda_{\mathrm{X}^{+}}^0=74.0 \mathrm{~S} \mathrm{~cm}^2 \mathrm{~mol}^{-1} )

  • A.

    76.0

  • B.

    80.0

  • C.

    100.0

  • D.

    90.0

Answer: B
  1. Concept: For a strong electrolyte, the Debye-Hückel-Onsager equation describes how molar conductivity varies with concentration:
Λm=ΛmAc\Lambda_{\mathrm{m}} = \Lambda_{\mathrm{m}}^{\circ} - A\sqrt{c}

where Λm\Lambda_{\mathrm{m}}^{\circ} is the limiting molar conductivity and AA is the given slope (with a negative sign already built into the equation).

  1. Finding c\sqrt{c}: since c=0.01 Mc = 0.01\ \mathrm{M},
c=0.01=0.1\sqrt{c} = \sqrt{0.01} = 0.1
  1. Substituting the known values Λm=145.0\Lambda_{\mathrm{m}} = 145.0 and slope =90.0= -90.0:
145.0=Λm90.0×0.1145.0 = \Lambda_{\mathrm{m}}^{\circ} - 90.0 \times 0.1 Λm=145.0+9.0=154.0 S cm2 mol1\Lambda_{\mathrm{m}}^{\circ} = 145.0 + 9.0 = 154.0\ \mathrm{S\ cm^2\ mol^{-1}}
  1. Using Kohlrausch's law of independent migration of ions: the limiting molar conductivity of a salt is the sum of the limiting ionic conductivities of its ions.
λm(XY)=λX++λY\lambda_{\mathrm{m(XY)}}^{\circ} = \lambda_{\mathrm{X}^{+}}^{\circ} + \lambda_{\mathrm{Y}^{-}}^{\circ} 154.0=74.0+λY154.0 = 74.0 + \lambda_{\mathrm{Y}^{-}}^{\circ} λY=80.0 S cm2 mol1\lambda_{\mathrm{Y}^{-}}^{\circ} = 80.0\ \mathrm{S\ cm^2\ mol^{-1}}

Hence, the answer is Option B: 80.0.

Q2 · 2026

A solution of copper sulphate is electrolysed for 10 minutes with a current of 1.5 amperes. The mass of copper deposited at cathode is : (Given : Molar mass of Cu=63 g mol1\mathrm{Cu}=63 \mathrm{~g} \mathrm{~mol}^{-1}; 1 F=96487C mol1)\left.1 \mathrm{~F}=96487 \mathrm{C} \mathrm{~mol}^{-1}\right)

  • A.

    1.7018 g

  • B.

    0.2938 g

  • C.

    2.4036 g

  • D.

    0.5876 g

Answer: B
  1. Understanding the setup: When CuSO4\mathrm{CuSO}_4 is electrolysed, Cu2+\mathrm{Cu}^{2+} ions move to the cathode and gain electrons to form copper metal:
Cu2++2eCu(s)\mathrm{Cu}^{2+} + 2e^- \rightarrow \mathrm{Cu(s)}

Since 2 electrons are needed per copper atom, n=2n = 2.

  1. Applying Faraday's law: the mass deposited depends on the molar mass, the current, and the time, according to:
W=M×I×tn×FW = \frac{M \times I \times t}{n \times F}
  1. Converting time to seconds: t=10×60=600 st = 10 \times 60 = 600\ \mathrm{s}, and using I=1.5 AI = 1.5\ \mathrm{A}, M=63 g/molM = 63\ \mathrm{g/mol}:
W=63×1.5×6002×96487W = \frac{63 \times 1.5 \times 600}{2 \times 96487}
  1. Calculating the result:
W=567001929740.2938 gW = \frac{56700}{192974} \approx 0.2938\ \mathrm{g}

Hence, the answer is Option B: 0.2938 g.

Q3 · 2026

Calculate emf of the half cell given below : Pt( s)H2( g,2 atm)HCl(aq,0.02M)EH2/H+=0 V\begin{aligned} & \mathrm{Pt}(\mathrm{~s})\left|\mathrm{H}_2(\mathrm{~g}, 2 \mathrm{~atm})\right| \mathrm{HCl}(\mathrm{aq}, 0.02 \mathrm{M}) \\ & \mathrm{E}_{\mathrm{H}_2 / \mathrm{H}^{+}}^{\circ}=0 \mathrm{~V} \end{aligned} (Given: 2.303RTF=0.059,log2=0.3010\frac{2.303 R T}{F}=0.059, \log 2=0.3010 )

  • A.

    -0.109 V

  • B.

    0.035 V

  • C.

    -0.035 V

  • D.

    0.109 V

Answer: D
  1. Writing the electrode reaction: at this electrode, hydrogen gas is oxidised to hydrogen ions:
H2( g)2H+(aq)+2e\mathrm{H}_2(\mathrm{~g}) \rightarrow 2\mathrm{H}^{+}(\mathrm{aq}) + 2e^-

Since 2 electrons are transferred, n=2n = 2.

  1. Applying the Nernst equation: this equation adjusts the standard potential EE^\circ for the actual concentrations and pressures present:
E=E2.303RTnFlog[H+]2PH2E = E^\circ - \frac{2.303RT}{nF}\log\frac{[\mathrm{H}^+]^2}{P_{\mathrm{H}_2}}
  1. Substituting the known values: E=0E^\circ = 0, [H+]=0.02 M[\mathrm{H}^+] = 0.02\ \mathrm{M}, PH2=2 atmP_{\mathrm{H}_2} = 2\ \mathrm{atm}, and 2.303RTF=0.059\frac{2.303RT}{F} = 0.059:
E=00.0592log(0.02)22E = 0 - \frac{0.059}{2}\log\frac{(0.02)^2}{2}
  1. Simplifying the term inside the logarithm:
(0.02)22=0.00042=2×104\frac{(0.02)^2}{2} = \frac{0.0004}{2} = 2\times10^{-4} E=0.0295log(2×104)E = -0.0295 \log(2\times10^{-4})
  1. Splitting the logarithm using log(a×b)=loga+logb\log(a\times b) = \log a + \log b, with log2=0.3010\log 2 = 0.3010 and log104=4\log 10^{-4} = -4:
E=0.0295(0.30104)=0.0295(3.699)E = -0.0295(0.3010 - 4) = -0.0295(-3.699) E=0.109 VE = 0.109\ \mathrm{V}

Hence, the answer is Option D: 0.109 V.

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