For the following problem, use a separate sheet of paper for…
For the following problem, use a separate sheet of paper for your answer and then upload your answers at the following link: https://canvas.dccc.edu/courses/28473/assignments/574397 Your work must be shown for full credit. A C8H14 hydrocarbon (A) is reduced by sodium in liquid ammonia to a single C8H16 product (B). Both compounds undergo hydrogenation (using a Pt catalyst) to give 2,5-dimethylhexane. Ozonolysis of B followed by oxidative workup with H2O2 produces a single C4H8O2 carboxylic acid. Reaction of B with peroxybenzoic acid (C6H5CO3H) gives a chiral C8H14O product (C), but reaction with bromine gives an achiral C8H14Br2 product (D). Draw the structures for A, B, C, and D and show how you arrived at your answers using chemical equations.