Question

I have most of the information, but I need help to organize it based on the prompts below the pictures.

laughlin Mass spec 984 pale ve N45 Whit Snow Relative Intensity tood for ved Stirre MW E 25 50 75 125 150 100 m/ neon Om belo

H-RUMR dddd dd TH PPM C-NMR RCH₂OH 100 80 60 40 PPM 140 120 R₂ C = Chi 200 RCH 2I

Date Mass Specta: Peak at m/2 = 134 is base peak molecular weight of compound. indicate IR specta: 3000 cmt 11200 cmt Indicat

Mass Spec

Molecular Weight:

Important Fragments; what are they and what do they mean? (base peak structure, is there a halogen, is there a benzene ring, is there an odd number of nitrogens, other important fragments that tell something about the structure)

IR

Is there an OH? Wavenumber?

Is there a carbonyl group? If so what type (acid. ester, amide, aldehyde, ketone etc.)?   Wave number?

Other important peaks (terminal alkyne, cyano group, aromatic, alkene, nitro group, amine etc.) and where are they?

1H-NMR

Identify every signal; chemical shift, what is it due to( i.e what type of proton, aromatic, aldehydic, O-H, N-H, vinyl etc.) and how many protons does it represent.

13C-NMR

How many different types of carbons are present?

What type of carbon does each signal represent?

How can you put the skeleton together?

LOGIC:

Carefully, and thoroughly show how you used the spectral data to determine your structure. Show how all your data confirms your structure. Especially useful is using 1H-NMR as confirmation.

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Answer #1

• Forom Mass spectroscopy => Molecular ion peak = 134 from IR peak N3000 an pear w2gooum peak N 1100cm - C(502) - 11 stretchi

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