With three bonds to each of two other molecules it should be very strong.
2006-07-25 03:04:31 · 4 answers · asked by Fredrick Carley 2 in Science & Mathematics ➔ Chemistry
because the bond is deloclised , it was observed by kekula C-C bond length is 1.54 Ao and C=C is 1.39 Ao but C-C bondlenth in benzene is 1.39 Ao in between doulbe and single bond .
2006-07-25 03:15:49 · answer #1 · answered by Jitendra P 1 · 3⤊ 0⤋
You can polymerize benzene as a phenyl group but not using the distributed double bonds of the ring. Esterfication is a common way of polymerizing R-Ph. R is whatever is attached to the benzene ring, and Ph is the benzene ring (called phenyl). If the R has an alcohol group at one end and an acid group at the other you can polymerize the R-Ph by esterfication. Common process of polymerization. You can also make polyphenyl thioether (PPS) with a thio group (contains sulfur).
2006-07-25 07:08:21 · answer #2 · answered by Alan Turing 5 · 0⤊ 0⤋
To extend...because the double bonds in benzene are delocalized, they are much more stable that isolated, non-delocalized double bonds. As a result, beneze is really a rather stable compound with very little tendency to react.
2006-07-25 03:21:11 · answer #3 · answered by hcbiochem 7 · 0⤊ 0⤋
because it's really hard to get benze to react at all. it's very stable as it is with the delocalized bond
2006-07-25 08:52:55 · answer #4 · answered by shiara_blade 6 · 0⤊ 0⤋