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:
ΔH°rxn = - 433.1 KJ/mol
Explanation:
- CH4(g) + 4Cl2(g) → CCl4(g) + 4HCl(g)
⇒ ΔH°rxn = 4ΔH°HCl(g) + ΔH°CCl4(g) - 4ΔH°Cl2(g) - ΔH°CH4(g)
∴ ΔH°Cl2(g) = 0 KJ/mol.....pure element in its reference state
∴ ΔH°CCl4(g) = - 138.7 KJ/mol
∴ ΔH°HCl(g) = - 92.3 KJ/mol
∴ ΔH°CH4(g) = - 74.8 KJ/mol
⇒ ΔH°rxn = 4(- 92.3 KJ/mol) + (- 138.7 KJ/mol) - 4(0 KJ/mol) - (- 74.8 KJ/mol)
⇒ ΔH°rxn = - 369.2 KJ/mol - 138.7 KJ/mol - 0 KJ/mol + 74.8 KJ/mol
⇒ ΔH°rxn = - 433.1 KJ/mol
Explanation:
To form bonds with noble gases, a lot of energy is required to form those bonds. Halogens, on the other hand, are extremely reactive. ... The halogens tend to be very reactive, while the noble gases are in no way reactive and don't bond easily, if at all.
The solute is sodium chloride seeing as it is being dissolved. The solvent would be water.