Experiment 16 Grignard Reaction with a Ketone Triphenylmethanol

Given the data tabulated below for the rate of reaction of maleic anhydride with a series of substituted 1,3-butadienes, offer a reasonable explanation to account for the trend in the rates. [Pg.275]

Predict the structure of the product formed in the following reactions. [Pg.275]

Offer an explanation of why anthracene preferentially forms a Diels-Alder adduct at the 9,10 positions. [Pg.275]

Experiment [31] demonstrates the monobromination of anthracene to yield one specific monosubstituted product. Other conditions may be used to form other monobrominated anthracenes. Draw the structures of, and name, the possible monobromo-substituted anthracenes that could be prepared in the laboratory. [Pg.275]

There are four reasonable resonance structures for anthracene. Draw them. [Pg.275]

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