The answer to your question is nitrogen dioxide
Answer:
Lewis structure for nitrogen triiodide,
is given in the attachment.
Explanation:
Given:
The given compound is Nitrogen triiodide. In which 1 atom of Nitrogen combines with 3 atoms of Iodine. Both Nitrogen and Iodine are non-metals,So they form covalent bond by sharing of electrons.
The electron configuration of Nitrogen and Iodine is given below;

There are 5 electrons in valance shell of Nitrogen atom and 7 electrons in valance shell of Iodine atom.
So, 3 atom of Iodine shares 1 electron with 1 electrons of Nitrogen.
The Lewis dot Structure is in the attachment.
Answer:
The most stable conformer would be the anti-conformer when the substituent methyl groups are farthest away from each other.
Explanation:
Isomers are chemical compounds with the same molecular formula but with different molecular structures.
Conformers are a special type of isomers that produce different structures when the substituents of a Carbon-Carbon single bond (C-C) are rotated.
In 2,3 dimethyl butane, the substituent methyl groups are located around the second and third Carbon to Carbon single bond.
To achieve a stable configuration, the methyl group substituents need to be as far apart as possible (that is, in an anti-position) to minimise repulsion.
The closer the methyl groups are to each other, the more they repel each other and the more unstable the conformer becomes.
Answer:
C) 5.6
Explanation:
From Henderson-Hasselbalch equation:

A = Conjugate base, HA = Acid
%A = 0.251 / (0.251 + 0.1) = 20%, hence %HA = 80%
100 mL of a 0.2 M = 0.02 mol
base = 20% of 0.02 = 0.004
Acid = 80% of 0.02 = 0.016
0.004 moles of base will get protonated by .004 moles of H+ from HCl, forming 0.004 moles of acid
0.02mol original acid - .004 mol H+ = 0.016 mol of conjugate base
Hence A/HA = 0.016/0.004
Since the new pH is 6.2, therefore: