Consider the 1H NMR spectrum for the following compound: CH3CH2CH3
Predict the first-order splitting patterns of the indicated proton. This question uses specific splitting patterns instead of the often used generic term "multiplet."
a. doublet of quartets
b. triplet of triplets
c. septet
d. quartet of quartets
e. quintet

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!

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