| List I | List II | ||
| (A) | Weak intermolecular forces of attraction | I | Hexamethylenedia mine + adipic acid |
| (B) | Hydrogen bonding | II | AlEt3 + TiCl4 |
| (C) | Heavily branched polymer | III | 2-chloro-1, 3-butadiene |
| (D) | High density polymer | III | phenol+ formaldehyde |
choose the correct answer from the options given below:
1. A. Weak intermolecular forces of attraction: 2–chloro–1,3–butadiene (chloroprene) is the monomer of neoprene, which has weak intermolecular forces of attraction, being an elastomer. Correct match: III. 2–chloro–1,3–butadiene.
2. B. Hydrogen bonding: Hexamethylenediamine reacts with adipic acid to form Nylon-6,6. The presence of the amide group allows hydrogen bonding between polymer chains. Correct match: I. Hexamethylenediamine + adipic acid.
3. C. Heavily branched polymer: - Phenol reacts with formaldehyde to form Bakelite, which is a heavily branched (cross-linked) polymer. Correct match: IV. Phenol + formaldehyde.
4. D. High density polymer: - High-density polyethylene is prepared using the Ziegler-Natta catalyst (\( \text{AlEt}_3 + \text{TiCl}_4 \)). Correct match: II. \( \text{AlEt}_3 + \text{TiCl}_4 \). ### Final Matching: \[ \text{A–III, B–I, C–IV, D–II.} \]
Calculate the potential for half-cell containing 0.01 M K\(_2\)Cr\(_2\)O\(_7\)(aq), 0.01 M Cr\(^{3+}\)(aq), and 1.0 x 10\(^{-4}\) M H\(^+\)(aq).



In the first configuration (1) as shown in the figure, four identical charges \( q_0 \) are kept at the corners A, B, C and D of square of side length \( a \). In the second configuration (2), the same charges are shifted to mid points C, E, H, and F of the square. If \( K = \frac{1}{4\pi \epsilon_0} \), the difference between the potential energies of configuration (2) and (1) is given by: