Answer:
(3R,4R)-4-bromohexan-3-ol
Explanation:
In this case, we have reaction called <u>halohydrin formation</u>. This is a <u>markovnikov reaction</u> with <u>anti configuration</u>. Therefore the halogen in this case "Br" and the "OH" must have <u>different configurations</u>. Additionally, in this molecule both carbons have the <u>same substitution</u>, so the "OH" can go in any carbon.
Finally, in the product we will have <u>chiral carbons</u>, so we have to find the absolute configuration for each carbon. On carbon 3 we will have an "R" configuration on carbon 4 we will have also an "R" configuration. (See figure 1)
I hope it helps!
Answer: No
Explanation: <em>Reactants</em> are the substances present at the beginning of a chemical reaction. In the burning of natural gas, for example, methane (CH4) and oxygen (O2) are the reactants in the chemical reaction. <em>Products </em>are the substances formed by a chemical reaction. In the burning of natural gas, carbon dioxide (CO2) and water (H2O) are the products formed by the reaction.
Answer:
Ether
SN1 mechanism
Explanation:
The nucleophile in this reaction is CH3OH. It is a poor nucleopile. We already know that a poor nucleophile reacting with a tertiary alkyl halide often leads to the substitution product as the major product.
Also, the iodide ion is a good leaving group. This makes the SN1 substitution more likely yielding the ether as the major product as shown in the image attached.