Please answer all of number 1 completely please. Thanks

C. Sample bottle labeled with name, date, product name, mass, and MP Questions: 1. Some possible side reactions can happen to the Grignard reagent. Draw reactions to show what would happen if: a. It reacts with moisture (or anything protic) b. It has a coupling reaction with unreacted bromobenzene It reacts with carbon dioxide from air d. Not enough Grignard reagent formed to react with all the methyl benzoate while doing Procedure B. 2. What step(s) in the workup remove each of the side products? What about left-over reactants? 3. What peaks in the IR (present or absent) show that you have the correct product and not leftover reactant? 4. Usually, we use hydrochloric acid instead of sulfuric acid in the workups. What other product might form if you used HCl instead of H2SO4 in the first workup step (above)? 5. What happened when the triphenylmethanol reacts with the sulfuric acid? Is the reaction reversible? 6. Compare TLC results: a. Was there a spot showing residual triphenylmethanol from the second plate? b. Were there any spots you couldn't attribute to product, biphenyl, or benzophenone? If so, try to guess what they might have been. Remember that low polarity molecules will have a higher Rithan polar molecules