Abusive head trauma is usually associated with a parent or caregiver becoming angry or frustrated.
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<span>1,3-cylohexadiene i synthesized starting from cyclohexane in following 4 steps.
1) Free Radical Substitution Rxn: Halogenation of cyclohexane in the presence of UV yield chlorocyclohexane.
2) Elimination Rxn: Dehydrohalogenation of chlorocyclohexane yields cyclohexene.
3) Halogenation of Cyclohexene (Electrophillic Addition Rxn) gives 1,2-dihalocyclohexane.
4) Elemination Rxn: When dibromocyclohexane is treated with KOH and heated it gives 1,3-cyclohexadiene as shown below,</span>
1) Free Radical Substitution Rxn: Halogenation of cyclohexane in the presence of UV yield chlorocyclohexane.
2) Elimination Rxn: Dehydrohalogenation of chlorocyclohexane yields cyclohexene.
3) Halogenation of Cyclohexene (Electrophillic Addition Rxn) gives 1,2-dihalocyclohexane.
4) Elemination Rxn: When dibromocyclohexane is treated with KOH and heated it gives 1,3-cyclohexadiene as shown below,</span>
Answer:
(3R,4R)-4-bromohexan-3-ol
Explanation:
In this case, we have reaction called <u>halohydrin formation</u>. This is a <u>markovnikov reaction</u> with <u>anti configuration</u>. Therefore the halogen in this case "Br" and the "OH" must have <u>different configurations</u>. Additionally, in this molecule both carbons have the <u>same substitution</u>, so the "OH" can go in any carbon.
Finally, in the product we will have <u>chiral carbons</u>, so we have to find the absolute configuration for each carbon. On carbon 3 we will have an "R" configuration on carbon 4 we will have also an "R" configuration. (See figure 1)
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