Chapter 18: Q 51. (page 723)
Question: Using resonance structures, explain why a nitroso group (-NO) is an ortho, para director that deactivates a benzene ring toward electrophilic attack.
Short Answer
Answer
Chapter 18: Q 51. (page 723)
Question: Using resonance structures, explain why a nitroso group (-NO) is an ortho, para director that deactivates a benzene ring toward electrophilic attack.
Answer
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Get started for freeWhich substituents have an electron-withdrawing and which have an electron-donating inductive effect
a
b
c
What is the major product formed by an intramolecular FriedelโCrafts acylation of the following compound?
Draw the products of each reaction.
For each N-substituted benzene, predict whether the compound reacts faster than, slower than, or at a similar rate to benzene in electrophilic aromatic substitution. Then draw the major product (s) formed when each compound reacts with a general electrophile .
Question: Reaction of p-cresol with two equivalents of 2-methylprop-1-ene affords BHT, a preservative with molecular formula . BHT gives the following NMR spectral data: 1.4 (singlet, 18 H), 2.27 (singlet, 3 H), 5.0 (singlet, 1 H), and 7.0 (singlet, 2 H) ppm. What is the structure of BHT? Draw a stepwise mechanism illustrating how it is formed
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