Question

14,15,16,17,18

14. Provide the major organic product of the reaction below 2 CHIS 15. Draw the major organic product venerated in the reaction below. Pay particular attention to regio- and stereochemical detail. 1.0, 2. (CH 16. Addition of HCl to 3-methyl-1-butene yields a mixture of two constitutional alkyl chloride isomers. What are they likely to be and how are they formed? Give detailed equations. 17. If stereoisomers are considered, how many alkyl chlorides from #16, could be products? 18. Give the structures and names of the principal products expected from the addition of Hito: (consider only constitutional isomers) a) 2-butene b) 2-pentene c) 2-methyl-1-butene d) 2-methyl-2-butene e) 2,3-dimethyl-1-butene f) 2,4,4-trimethyl-2-pentene

Answer 1

Ozonolysis of alkene gives Carbonyl Compounds.

OsO4 is a selective syn dihydroxylation reagent.

Addition of HI by Markonikoff addition

Hale you 18) a. HI - 2.10 do but one 2-todo Pentane 2-iodo-2-methys but ane HI ID 1-2-methyl butane - 2 lado-2-methur e) L M 41, #7 - 2-10do-pod-dimethy) bu taux i 2 2-vodo-2, trimethyl Penta ne P