Utilisateur
only cooh
coo-na+. +h20
(coo-)2mg +h2
h+
it can attract cl2 more easily
sidewwys overlap of p orbitals
hesd on overlwp of p orbitals
both involve the overlappimf of p orbitwls
1) kekule consiste of slternwtimg pi bomds whereas the deloclaised model has the pi bonds delocalised wcross the whole ring
1) it does not discoloursie bromine water
2) the dehyrogenwtioj of cyclohexene is -120kjmol so we would expect the dehdrogenetwtiom of benzene ro be -360 but ir is actyally less exothermic thsn oredicted
a known database
H+ /KCN
si(ch3)4
major product formed from more stable cwrbocwtion
nh3+
work it out then add the remaining mr for what is not included in the polyester
no
only carobylic acid
both phenol and csrbocylic acid
- further wubsitution mwy occur
- subisituion ,ay occur on any cwrbin atom in the cwrbon chwin
to idemtify oh or nh protons
either nh2 or nh3 plus
bresking of covalent bond in which each atom recovd 1 electron from the bonding pair
pi has a weaker
1
cwrboxylic acids amd phemols
not alchols
only carboylic acids
overlap of obitals between bonding atoms
sideways overlap of adjecent orbiatls
super non imposbsle mirror images around a chiral carbon
H+/H20