Answer:
Reagents: 1) 
2) 
, 
Mechanism: Hydroboration
Explanation:
In this case, we have a <u>hydration of alkene</u>s reaction. But, in this example, we have an <u>anti-Markovnikov reaction</u>. In other words, the "OH" is added in the least substituted carbon. Therefore we have to choose an anti-Markovnikov reaction: <u>"hydroboration"</u>.
The <u>first step</u> of this reaction is the addition of borane () to the double bond. Then in the <u>second step</u>, we have the deprotonation of the hydrogen peroxide, to obtain the peroxide anion. In the <u>third step</u>, the peroxide anion attacks the molecule produced in the first step to produce a complex compound in which we have a bond "
". In <u>step number 4</u> we have the migration of the C-B bond to oxygen. Then in <u>step number 5</u>, we have the attack of on the 
to produce an alkoxide. Finally, the water molecule produce in step 2 will <u>protonate</u> the molecule to produce the alcohol.
See figure 1
I hope it helps!
Answer:
The p orbital can hold up to six electrons. We'll put six in the 2p orbital and then put the remaining electron in the 3s. Therefore the sodium electron configuration will be 1s22s22p63s1.
Explanation:
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