17. Draw the molecular orbital diagrams for a photochemical (hv) reaction between two molecules of ethylene (2+2). Based on your diagrams, is the reaction viable under the photochemical condition? CH₂ CH₂ H₂C 18. Draw a mechanism for the EAS reaction between tertbutyl benzene and acetyl chloride. For full points please show important resonance structures for the electrophilic species (acylium ion). sure to indicate the structure of the final product in the drawing of your mechanism. CH3 CH3 CH₂ H3C hv CI AICI 19. Devise a synthesis using reagents from Organic Chemistry 1 and new reactions from Organic Chemistry 2. The three reaction arrows do not mean only three steps are required (it could be three steps, but not necessarily). Br CH₂

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17.
Draw the molecular orbital diagrams for a photochemical (hv) reaction between two
molecules of ethylene (2+2). Based on your diagrams, is the reaction viable under the photochemical
condition?
CH₂
CH₂
H₂C
18.
Draw a mechanism for the EAS reaction between tertbutyl benzene and acetyl chloride.
For full points please show important resonance structures for the electrophilic species (acylium ion). Be
sure to indicate the structure of the final product in the drawing of your mechanism.
CH3
CH3
+
CH₂
CH₂
H₂C
hv
AICI,
19.
Devise a synthesis using reagents from Organic Chemistry 1 and new reactions from
Organic Chemistry 2. The three reaction arrows do not mean only three steps are required (it could be
three steps, but not necessarily).
Br
CH₂
Transcribed Image Text:17. Draw the molecular orbital diagrams for a photochemical (hv) reaction between two molecules of ethylene (2+2). Based on your diagrams, is the reaction viable under the photochemical condition? CH₂ CH₂ H₂C 18. Draw a mechanism for the EAS reaction between tertbutyl benzene and acetyl chloride. For full points please show important resonance structures for the electrophilic species (acylium ion). Be sure to indicate the structure of the final product in the drawing of your mechanism. CH3 CH3 + CH₂ CH₂ H₂C hv AICI, 19. Devise a synthesis using reagents from Organic Chemistry 1 and new reactions from Organic Chemistry 2. The three reaction arrows do not mean only three steps are required (it could be three steps, but not necessarily). Br CH₂
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