ANSWER CHOICES ARE BELOW:-

The compound that yielded the IR spectra below most likely has a due to the . a table of common IR shifts is included for your convenience. IR Absorptions of Common Functional Groups \begin{tabular}{lll} \hline Functional Group & Absorption Location (cm1) & Absorption Intensity \\ \hline Alkane (CH) & 2,8502,975 & Medium to strong \\ \hline Alcohol (OH) & 3,4003,700 & Strong, broad \\ \hline Alkene (C=C) & 1,6401,680 & Weak to medium \\ (C=CH) & 3,0203,100 & Medium \\ \hline Alkyne & & \\ (C=C) & 2,1002,250 & Medium \\ (C=CH) & 3,300 & Strong \\ \hline Nitrile (C=N) & 2,2002,250 & Medium \\ \hline Aromatics & 1,6502,000 & Weak \\ \hline Amines (N-H) & 3,3003,350 & Medium \\ \hline Carbonyls (C=0) & & Strong \\ Aldehyde (CHO) & 1,7201,740 & \\ Ketone (RCOR) & 1,715 & \\ Ester (RCOOR) & 1,7351,750 & \\ Acid (RCOOH) & 1,7001,725 & \\ \hline \end{tabular} The compound that yielded the IR spectra below most likely has : due to the . a table of common II convenience. ue to the [Select] broad peak at 3300 which correlates to an 0H bond + a sharp peak at 1700 that correlates to a carbonyl broad peak at 3300 which correlates to an OH bond the CH stretch at 3100