Chapter 15: Q15-15-27 (page 477)
Look at the five resonance structures for phenanthrene (Problem 15-26), and predict which of its carbon-carbon bonds is the shortest.
Short Answer
Shorter bond at 6 and 7 carbon
Chapter 15: Q15-15-27 (page 477)
Look at the five resonance structures for phenanthrene (Problem 15-26), and predict which of its carbon-carbon bonds is the shortest.
Shorter bond at 6 and 7 carbon
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Get started for freeGive IUPAC names for the following compounds
a)
How might you convert 1, 3, 5, 7-cyclononatetraene to an aromatic substance?
Azulene, a beautiful blue hydrocarbon, is an isomer of naphthalene. Is azulene aromatic? Draw a second resonance form of azulene in addition to that shown.
Azo dyes are the major source of artificial color in textiles and food. Part of the reason for their intense coloring is the conjugation from an electron-donating group through the diazo bridge to an electron-withdrawing group on the other side. For the azo dyes below, draw a resonance form that shows how the electron-donating group is related to the electron-withdrawing group on the other side of the diazo bridge. Used curved arrows to show how the electrons are reorganized.
a.
Methyl orange
b.
C.I. Acid Red 74
Draw structures corresponding to the following names:
(a) 3-Methyl-1,2-benzenediamine
(b) 1,3,5-Benzenetriol
(c) 3-Methyl-2-phenylhexane
(d) o-Aminobenzoic acid
(e) m-Bromophenol
(f) 2,4,6-Trinitrophenol (picric acid)
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