Answer:
a. 3-methylbutan-2-ol
b. 2-methylcyclohexan-1-ol
Explanation:
For this reaction, we must remember that the hydroboration is an <u>"anti-Markovnikov" reaction</u>. This means that the "OH" will be added at the <em>least substituted carbon of the double bond.</em>
In the case of <u>2-methyl-2-butene</u>, the double bond is between carbons 2 and 3. Carbon 2 has two bonds with two methyls and carbon 3 is attached to 1 carbon. Therefore <u>the "OH" will be added to carbon three</u> producing <u>3-methylbutan-2-ol</u>.
For 1-methylcyclohexene, the double bond is between carbons 1 and 2. Carbon 1 is attached to two carbons (carbons 6 and 7) and carbon 2 is attached to one carbon (carbon 3). Therefore<u> the "OH" will be added to carbon 2</u> producing <u>2-methylcyclohexan-1-ol</u>.
See figure 1
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The group on the periodic table that would have 0 electronegativity due to the fact that their valence shell is full, i.e, have a full octet would be the inert or noble gases. They have a total of 8 electrons in their valence shell and are thus inert and cannot strongly attract electrons toward itself, from neighbouring atom electrons as it does not need to.
3Na2O(at) + 2Al(NO3)3(aq) —> 6NaNO3(aq) + Al2O3(s)
This is a double replacement reaction and NaNO3 is aqueous because Na is an alkali metal, plus nitrate is in the solution. Both of these are soluble. Al2O3 is not soluble because it does not contain any element that is soluble and is hence the precipitate.
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POH = - log [ OH⁻ ]
pOH = - log [ 1 x 10⁻⁹ ]
pOH = 9
Answer C
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