J. J. Thomson's plum pudding model was based on all BUT one of these beliefs. That is
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Answer:
The simulated 1H NMR spectrum for ethyl acetate is shown in the drawing attached.
Explanation:
To construct this NMR it is necessary to identify the essential components that can produce resonance peaks.
Two main groups can be identified, the acetyl group containing a sub-component (CH3) capable of producing a resonance peak, and the ethyl group containing two components (CH2 and CH3) each of which can produce on its own its own resonance peak.
This is a two step step reaction as shown below,
Step 1:
Epoxidation of Alkene:
In first step Cyclohexene is treated with peroxybenzoic acid in the presence of Dichloromethane which results in the formation of epoxide moiety.
Step 2:
Nucleophillic Substitution Reaction:
In second step the epoxide formed is treated with Sodium Methoxide which acts as a nucleophile and attacks the less hindered carbon of epoxide resulting in the formation of final product as shown below.
Step 1:
Epoxidation of Alkene:
In first step Cyclohexene is treated with peroxybenzoic acid in the presence of Dichloromethane which results in the formation of epoxide moiety.
Step 2:
Nucleophillic Substitution Reaction:
In second step the epoxide formed is treated with Sodium Methoxide which acts as a nucleophile and attacks the less hindered carbon of epoxide resulting in the formation of final product as shown below.