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i have this base
.............N(:)H
..............||
H2N(:) -C-N(:)H2 + H+

which site is more basic when you add H+, explain your choice using resonance structure

note (:) is one lone pair on N

2007-09-12 13:54:40 · 2 answers · asked by jennifer 2 in Science & Mathematics Chemistry

.................... is nothing i just used it to control my bonding to be the right position

2007-09-12 13:56:00 · update #1

2 answers

It might help if you name the compound. You seem to have a guanidino group, (H2N)2C=NH + H+ ===> -C(NH2)3+, with the (+) distributed by resonance amongf the three N's.

2007-09-12 14:04:58 · answer #1 · answered by steve_geo1 7 · 1 0

A cyclic hydrocarbon is a hydrocarbon wherein the 1st carbon is suitable to the perfect hydrocarbon, and hence the smallest cyclic hydrocarbon has 3 carbons. An aliphatic compound is truthfully any hydrocarbon devoid of aromaticity; it fairly is, there is not any delocalized pi orbitals on the cyclic compound (ie benzene-like resonance). So it fairly is an alkene, alkane, alkyne, cyclic hydrocarbon, etc as long because of the fact this is fairly not aromatic. i've got have been given in no way heard of alicyclic compounds until at last now...probable in basic terms cyclic hydrocarbons that are certainly no longer aromatic.

2016-11-15 02:13:44 · answer #2 · answered by ? 4 · 0 0

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