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: Although benzene itself absorbs at 128 ppm in its NMR spectrum, the carbons of substituted benzenes absorb either upfield or downfield from this value depending on the substituent. Explain the observed values for the carbon ortho to the given substituent in the monosubstituted benzene derivatives X and Y.
Question: Estimate where the protons bonded to the hybridized carbons will absorb in the 1 H NMR spectrum of each compound.
Question: a. Explain why protonation of pyrrole occurs at C2 to form A, rather than on the N atom toform B.
b. Explain why A is more acidic than C, the conjugate acid of pyridine.
Question: Early structural studies on benzene had to explain the following experimental evidence. When benzene was treated with (plus a Lewis acid), a single substitution product of molecular formula was formed. When this product was treated with another equivalent of , three different compounds of molecular formularole="math" localid="1648727281591" were formed.
Question: Explain why -pyrone reacts with to yield a substitution product (like benzene does),rather than an addition product to one of its bonds.
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