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
I hope it helps!
Every atom tends to form configuration of noble gas , with the 8 electrons in valence shell.
Answer: sharing
Reason: They do this to gain stability. The reason they don’t actually transfer is because the difference in electronegativity values are above a certain value.
Answer:
0.42%
Explanation:
<em>∵ pH = - log[H⁺].</em>
2.72 = - log[H⁺]
∴ [H⁺] = 1.905 x 10⁻³.
<em>∵ [H⁺] = √Ka.C</em>
∴ [H⁺]² = Ka.C
∴ ka = [H⁺]²/C = (1.905 x 10⁻³)²/(0.45) = 8.068 x 10⁻⁶.
<em>∵ Ka = α²C.</em>
Where, α is the degree of dissociation.
<em>∴ α = √(Ka/C) </em>= √(8.065 x 10⁻⁶/0.45) = <em>4.234 x 10⁻³.</em>
<em>∴ percentage ionization of the acid = α x 100</em> = (4.233 x 10⁻³)(100) = <em>0.4233% ≅ 0.42%.</em>