Explanation:
Bond order is inversely proportional to the bond length.
In 
molecule. one nitrogen is double bonded to nitrogen and one oxygen is single bonded to nitrogen and hydrogen bond.
- Bond order between the (N=O) bond is 2 which means that bond length between the (N=O) bond is shorter than that of the N-O bond.
- Bond order between the (N-O) bond is 1 which means that bond length of the N-O bond is longer than that of the bond length of (N=O) bond.
Answer: C excess reactant
Reason: It is not catalyst because catalyst are not consumed. It is not product because it was one of the reactants. It is not limiting because there was excess left over.
Answer:
See explanation and image attached
Explanation:
Aromatic compounds undergo electrophilic aromatic substitution reactions in which the aromatic ring is maintained.
Substituted benzenes may be more or less reactive towards electrophilic aromatic substitution than benzene depending on the nature of the substituent present in the ring.
Substituents that activate the ring towards electrophilic substitution such as -OCH3 are ortho-para directing.
The major products of the bromination of anisole are p-bromoanisole and o-bromoanisole. The resonance structures leading to these products are shown in the image attached.
