A C=O bond, displayed in answer D, has more distinct wave number and can't be mistaken for another type of bond. However a N-H bond, as is the case in answer C, has a wave number that overlaps with an O-H (alcohols) bond. Therefore D is the correct answer.
Which of the following could be distinguished from the other molecules due to the absence of a particularly distinct and characteristic peak?The question is asking for absence.
A) CH3CH2CH2CH2OH -Distinct peak at OH (of an alkanol)
B) CH3CH2CH2COOH -Distinct OH of an acid along side the C=O
C) CH3CH2CH2CH2NH2 -Distinct NH2
D) CH3CH2CH2COOCH3 -Have a look at it. Its got an ester linkage. Its got a C=O BUT so does B. Theres is nothing in D that differentiates it from B but theres the OH of the ACID in B that differentiates it from D.
Thats my take on it.
a N-H bond, as is the case in answer C, has a wave number that overlaps with an O-H (alcohols) bond.
Just to ask..why are you drawing comparison between the NH2 and the OH bonds? Sure, they overlap..but only when a compund contains these two functional groups. Neither of these 4 do..C) has only the NH2 so theres no OH that will affect it as you are suggesting. These compounds have their own distinct IR spectrum..I'm assuming theyre separate compunds run through the IR spectrophotometer at different times, not jumbled up.