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practiceexam2 - 1 a b c Br d O I F Cl 2 a(E)...

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1. Give the systematic name for each of the following chemicals: Cl F I Br O a) b) c) d) 2. Draw the following molecules: a) ( E )‐1‐bromo‐2‐methyl‐2‐butene b) 1‐chloro‐2,5‐cyclodiene c) 1‐bromo‐4‐methyl‐2‐pentyne d) ( 2E,4Z )‐2,4‐dichloro‐2,4‐heptadiene e) ( E )‐3‐iodo‐2‐pentene 3. Circle the more stable alkene. or or or a) b) c) 4. Draw curved arrows to show the flow of electrons responsible for the formation of the products shown. C C H H H H I C C H H H I H H O H H H O H H
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5. Draw the two‐step mechanism with curved arrows to show the reaction between cyclohexane and HBr. H Br 6. Indicate the hybridization and ideal bond angles for the following atoms in the boxes provided: OH HO O N O HN O P O O O O O P O O OH OH OH HO O 7. Label each as a nucleophile or electrophile. O H F H O H H H 8. Draw the expected product(s) or label as “NR” if no reaction would be expected to occur for the following:
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Cl H O H C OH HBr HCl H O + + + + + + 9.
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