chemistry to get this.? I am given the carbon-13 Nuclear Magnetic Resonance -- Off-Resonance deshielded experiment spectrum information as shown below, and asked to deduce the structure of the analyzed compound:
delta (ppm): triplet at 32.6, triplet at 118.8, and doublet at 134.2. C3H5Br
I'm assuming the triplet at 32.6 is from a -CH2, or more than one, but the only information I have for the other two peaks is C-C double bonds. It has 1 pi bond equivalence (nonsaturation number)... So, it should only have 1 double bond, right?
The question I asked is not the only thing I need answered... I really need someone to either explain this problem, or explain how to deduce the structures in general. Thanks!
delta (ppm): triplet at 32.6, triplet at 118.8, and doublet at 134.2. C3H5Br
I'm assuming the triplet at 32.6 is from a -CH2, or more than one, but the only information I have for the other two peaks is C-C double bonds. It has 1 pi bond equivalence (nonsaturation number)... So, it should only have 1 double bond, right?
The question I asked is not the only thing I need answered... I really need someone to either explain this problem, or explain how to deduce the structures in general. Thanks!