aqueous Magnesium Chloride reacts with liquid Bromide to form aqueous Magnesium Bromide and Chlorine gas
Heterogenous mixtures are unevenly mixed. Like oil and vinegar in vinaigrette if it is not emulsified well enough and they separate. Any case where two things are not evenly distributed within each other.
Homogenous mixtures are evenly mixed throughout. Like salt water or kool-aid (when it's mixed).
Hope this helps!
Hi, you have not provided structure of the aldehyde and alkoxide ion.
Therefore i'll show a mechanism corresponding to the proton transfer by considering a simple example.
Explanation: For an example, let's consider that proton transfer is taking place between a simple aldehyde e.g. acetaldehyde and a simple alkoxide base e.g. methoxide.
The hydrogen atom attached to the carbon atom adjacent to aldehyde group are most acidic. Hence they are removed by alkoxide preferably.
After removal of proton from aldehyde, a carbanion is generated. As it is a conjugated carbanion therefore the negative charge on carbon atom can conjugate through the carbonyl group to form an enolate which is another canonical form of the carbanion.
All the structures are shown below.
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!
Hydrogen i suppose is the right one