Answer:
The structure analysis says the compound must be Cumene or isopropylbenzene
Explanation:
Degree of unsaturation or double bond equivalent
D.B.E = [tex]C-\frac{H}{2}+\frac{N}{2}+1[/tex]
= [tex]9-\frac{12}{2}+\frac{0}{2}+1[/tex]
= 4
¹H NMR data analysis
(i) 1.2δ (doublet, I = 6H) two CH₃ are equivalents and the multiplicity says the neighboring carbon have one hydrogen.
(ii) 3.0δ (septet, I = 1H), one CH and the multiplicity says the neighboring carbon have six hydrogens.
(iii) 7.1δ (multiplet, I = 5H) , means
and the sturcture of the compound is