Chapter 17: Q.66. (page 641)
Question: Explain why compound A is much more stable than compound B.
Short Answer
Answer
The aromaticity of compound A makes it more stable than compound B.
Chapter 17: Q.66. (page 641)
Question: Explain why compound A is much more stable than compound B.
Answer
The aromaticity of compound A makes it more stable than compound B.
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Get started for freeQuestion: Use the inscribed polygon method to show why the cyclopentadienyl cation and radical are not aromatic.
Question: Januvia, the trade name for sitagliptin, was introduced in 2006 for the treatment of type 2 diabetes. (a) Explain why the five-membered ring in sitagliptin is aromatic. (b) Determine the hybridization of each N atom. (c) In what type of orbital does the lone pair on each N atom reside?
What orbitals are used to form the labeled bonds in the following molecule? Of the labeled bonds, which is the shortest?
Question: Draw the product formed when cyclohepta-1,3,5-triene (pKa = 39) is treated with a strong base. Why is its pKa so much higher than the pKa of cyclopentadiene?
Question: Treatment of indene with forms its conjugate base in a Brønsted–Lowry acid-base reaction. Draw all reasonable resonance structures for indene’s conjugate base, and explain why the of indene is lower than the of most hydrocarbons.
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