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!
Answer:
The attractive force between them decreases
Explanation:
This is because they become localised.
Answer:
Explanation:
By definition, <em>half neutralization</em> is the point at which half of the acid has been neutralized.
The neutralization reaction that you are studying is the acid-base reaction:
- HCl (aq) + NaOH (aq) → NaCl(aq) + H₂O (aq)
Then, since the starting molarity of the acid (HCl) is 0.2 M, you just need to find half of that concentration:
- Half molarity = M / 2 = 0.2 M / 2 = 0.1 M
So, the answer is the first choice: a. 0.1 M.
Answer:
transfer pipet that had markings every 0.1 mL.
Explanation:
a is the answer hope this helps