10.31 Triphenylmethane readily undergoes autooxidation to produce a hydroperoxide: c10s172 (a) Draw the expected hydroperoxide. (b) Explain why triphenylmethane is so susceptible to autooxidation. (c) In the presence of phenol (C6H5OH), triphenylmethane undergoes autooxidation at a much slower rate. Explain this observation.

C. definite shape, definite volume. that is a solid.

Answer    "a salt" would be the best answerexplanationsalts can be defined as ionic compounds that are neither acids nor bases. nacl is an example of a salt, and its ionic.an enzyme is an organic compound which is covalently bonded, not ionically bonded.acids are generally held together by covalent bondsan element does not need any bonds to exist

Adialysis unit requires 78.5 l of water.the estimated digit is 5.