The compound whose 1H NMR spectrum is shown has the molecular formula C8H9Br. Follow the following questions to predict the unknown structure.   3(a) Degree of the unsaturation of this compound = , 3(b) The two peaks at 3.16 δ and 3.56 δ indicate two triplets Yes or NO = 3(c) The compound has 2 CH2 groups Yes or No =  3(d) Depending on the two triplets' chemical shifts one of the CH2 may have attached to the Br, Yes or No =  3(e) The multiplet at 7.18 δ to 7.29 δ indicate that  compound is .........-disubstituted benzene =  3(f) The name of the unknown compound is =

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Chapter1: Chemical Foundations
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The compound whose 1H NMR spectrum is shown has the molecular formula C8H9Br. Follow the following questions to predict the unknown structure.

 

3(a) Degree of the unsaturation of this compound = ,

3(b) The two peaks at 3.16 δ and 3.56 δ indicate two triplets Yes or NO =

3(c) The compound has 2 CH2 groups Yes or No = 

3(d) Depending on the two triplets' chemical shifts one of the CH2 may have attached to the Br, Yes or No = 

3(e) The multiplet at 7.18 δ to 7.29 δ indicate that  compound is .........-disubstituted benzene = 

3(f) The name of the unknown compound is =

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