Heating the compound shown here at 225–235 °C for 8 h produced a new compound with the formula C23H16N,0. The mechanism for this reaction is believed to consist of a [4+2] cycloaddition followed by a [4+2] cycloelimination. The 'H NMR spectrum of the product contained the following signals: 8 8.33–8.25 and 7.58–6.97 (m, 14 H), 5.46 (s, 2 H). (a) Draw the mechanism for this reaction. (b) Draw the product. C6H5 C6H5 N. ? C23H16N20

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Chapter1: Chemical Foundations
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Heating the compound shown here at 225–235 °C
for 8 h produced a new compound with the formula
C23H16N,0. The mechanism for this reaction is believed
to consist of a [4+2] cycloaddition followed by a [4+2]
cycloelimination. The 'H NMR spectrum of the product
contained the following signals: 8 8.33–8.25 and
7.58–6.97 (m, 14 H), 5.46 (s, 2 H). (a) Draw the
mechanism for this reaction. (b) Draw the product.
C6H5
C6H5
N.
? C23H16N20
Transcribed Image Text:Heating the compound shown here at 225–235 °C for 8 h produced a new compound with the formula C23H16N,0. The mechanism for this reaction is believed to consist of a [4+2] cycloaddition followed by a [4+2] cycloelimination. The 'H NMR spectrum of the product contained the following signals: 8 8.33–8.25 and 7.58–6.97 (m, 14 H), 5.46 (s, 2 H). (a) Draw the mechanism for this reaction. (b) Draw the product. C6H5 C6H5 N. ? C23H16N20
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