if 6.1 ml of tert-butyl-chloride and a correct stoichiometric  molar ratio of biphenyl are involved in the friedel crafts alkylation reaction, what is the percent yield if 6.157 grams of tert-butylbiphenyl are synthesized and isolated? Round the answer to the nearest hundreth.

Label the infrared spectroscopy (IR) graphs based on the marked wavenumbers on the chart for tetraphenylcyclopentadienone (adol condensation with benzil and dibenzyl ketone) and tetraphenylhydrophathalic anhydride (by diels-alder reaction of previous product and maleic anhydride). Explain the differences between the two charts and determine if the experimental reactions were done successfully by comparing the experimental IR results shown with what you would expect the IR results to be. Attached is chart 1, chart 2, and respective reaction 1, reaction 2.

Rank each of the following compounds in decreasing order of reactivity towards Friedel-Crafts alkylation. Most reactive = 1; if a compound will not react, rank it as "non" rather than assigning a numerical value. Compound A: benzoic acid Compound B: aniline Compound C: anisole Compound D: phenol <

if 6.1 ml of tert butyl chloride and a correct stoichiometric molar ratio of biphenyl are involved in the friedel crafts alkylation reaction, how many grams of 4,4'-di-tert-butylbiphenyl are created if the reaction goes to completion with only the desired product forming? Round to the nerest hundreth.