Question

Consider the 1H NMR spectrum for the following compound:

Answer 1

Answer:

See explanation

Explanation:

In this case, we have to check the neighbors of each carbon in the molecule. In propane, we have two types of carbons (see figure 1) (blue and red ones). The red carbons are equivalent. (Both have the same neighbors). Now, we can analyze each carbon:

Blue carbon

In the blue carbon, we have 6 hydrogens neighbors (three on each methyl). If we follow the n+1 rule, we will have:

6+1= 7

For the blue carbon, we will have a Septet.

Red carbons

In the red carbon, we have only 2 neighbors (the carbon in the middle only have 2 hydrogens). If we follow the n+1 rule, we will have:

2+1=3

For the red carbon, we will have a triplet.

See figure 2

I hope it helps!