B is the right answer because it’s a double replacement reaction and the potassium is balanced with the sulphate
Answer:
Structures are given below.
Explanation:
- Treatment of 2-bromo-2-methylbutane with KOH in ethanol will give elimination of HBr through E2 mechanism.
- H atoms adjacent to Br will be eliminated.
- 2-bromo-2-methylbutane has two possible adjacent H atoms that can be eliminated giving mixture of products.
- Product of this elimination reaction is alkene. Here saytzeff fule is followed during elimination. So most substituted alkene will be major product.
- Structure of alkenes are given below.
Answer:
D-Glucose and L-Glucose
Explanation:
Aldohexose are the sugars which have six number of carbons and ends up in having an aldehyde group at one end. When dilute nitric acid is treated with any of them, the molecule gets oxidized (gets oxygen) and therefore turns into carboxylic acid.
The name of A is D-Glucose, and B is L-Glucose. Please find the structural formula attached.