В. i. Draw the possible conformations for trans-1,4-dibromocyclohexane. Show the most stable conformation. Also explain the reason for its stability. ii. Classify the following reagents as Lewis acids and Lewis bases. H;O, BF, AICI, CH,CH;NH; ii. Classify the following reagents as nucleophile and electrophiles. BF, CH,OH, CH,OCH, FeCl, iv. Classify the following reagents as oxidizing and reducing agents. O, NABH, LIAH4, KMNO,

3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOC1,. a) (CH3)»CCH;COH (CH3),CCH2CNHCH;CH=CH2 b) (CH3);CCH2COH (CH3);CCH2COCH,CH3

I'm having trouble trying to figure out where to move the doule bond, bc wherever I place it seems like it would violate the octet rule. can someone explain simply?

Fill in the blanks in the following SN2 reactions with either the appropriate nucleophile,electrophile, or product and include any stereochemistry where it is relevant.

Select reagents from the following table to bring about this conversion. a. HOCH₂ CH₂ OH, H+ 1. Os04 2. NaHSO3 RCO3 H H3O+ NaBH₁ b. (Enter your result as a string of letters, in the order that you wish to use the reagents, i.e. ade.) C. d. e. LOH f. g. HO dihydropyran, H+ 1. BH3 2. NaOH, H₂O, H2₂ O2 OH

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