Answer: negative acellaration or mass.
Explanation:
the first reason why is that i got that quistion right. and when objects are unbalanced it gives negative acellaration
Answer: option a and d
Explanation:
Option A- Benzene undergoes substitution reaction
Example : benzene reacts with chlorine to form chlorobenzene, in the presence of Iron
(iii) chloride as a catalyst
C6H6 + Cl2 ---> C6H5Cl + HCl
Option D- Benzene also undergoes addition reaction
Example: benzene reacts with hydrogen , in the presence of nickel as a catalyst to form
cyclohexane
C6H6 + 3H2 ---> C6H12
Reasons why Option B isn't the answer
Although benzeme has degree of unsaturation but it's not five degree of unsaturation.
Benzene has 6 carbon atoms and 4 degrees of unsaturation (1 ring and 3 double
bonds).
If you work backwards and double the degrees of unsaturation you have 8 degrees of
unsaturation instead of 5.
Option C - Benzene isn't a saturated hydrocarbon
For the neutralization process: an acid acts as a donor and donates protons to the base. On the other hand, the base acts as an acceptor and accepts the transferred protons. In a nutshell, neutralization is mainly proton transfer process.
As for the redox process: the oxidized material usually transfers electrons to the reduced material. In a nutshell, redox is mainly electron transfer process.
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!