Standard electrode potential for \( \text{Sn}^{4+}/\text{Sn}^{2+} \) couple is +0.15 V and that for the \( \text{Cr}^{3+}/\text{Cr} \) couple is -0.74 V. The two couples in their standard states are connected to make a cell. The cell potential will be:
To calculate the cell potential (\( E^\circ_{\text{cell}} \)), we use the standard electrode potentials of the given redox couples.
Given data:
\( E^\circ_{\text{Sn}^{4+}/\text{Sn}^{2+}} = +0.15V \)
\( E^\circ_{\text{Cr}^{3+}/\text{Cr}} = -0.74V \)
Step 1: Understanding the cell potential. The cell potential is calculated by subtracting the anode potential from the cathode potential. The two given standard electrode potentials are for the Sn^{4+}/Sn^{2+} couple (+0.15 V) and the Cr^{3+}/Cr couple (-0.74 V).
Step 2: Calculation. The cell potential is given by: \[ E_{\text{cell}} = E_{\text{cathode}} - E_{\text{anode}} = (+0.15 \, \text{V}) - (-0.74 \, \text{V}) = +0.89 \, \text{V} \]
Step 3: Conclusion. Thus, the cell potential is +0.89 V, corresponding to option (B). \vspace{10pt}
Write IUPAC names of the following compounds and classify them into primary, secondary and tertiary amines.
(i) (CH3 )2CHNH2 (ii) CH3 (CH2 )2NH2 (iii) CH3NHCH(CH3 )2
(iv) (CH3 )3CNH2 (v) C6H5NHCH3 (vi) (CH3CH2 )2NCH3 (vii) m–BrC6H4NH2
Give one chemical test to distinguish between the following pairs of compounds.
(i) Methylamine and dimethylamine
(ii) Secondary and tertiary amines
(iii) Ethylamine and aniline
(iv) Aniline and benzylamine
(v) Aniline and N-methylaniline
Account for the following:
(i) pKb of aniline is more than that of methylamine.
(ii) Ethylamine is soluble in water whereas aniline is not.
(iii) Methylamine in water reacts with ferric chloride to precipitate hydrated ferric oxide.
(iv) Although amino group is o– and p– directing in aromatic electrophilic substitution reactions, aniline on nitration gives a substantial amount of m-nitroaniline.
(v) Aniline does not undergo Friedel-Crafts reaction.
(vi) Diazonium salts of aromatic amines are more stable than those of aliphatic amines. (vii) Gabriel phthalimide synthesis is preferred for synthesising primary amines.