The Student Room Group
Reply 1
The carrier regenerates, you need cl2 and the mechanism is standard electrophillic aromatic substitution.
Reply 2
Sorry to interrupt someone elses thread but where do I find the mechanism for a standard elecrophilic aromatic substitution. I also wondered, can anyone explain to me the mechanism at the site below for Jones reagent oxidising alcohols?

acpcommunity.acp.edu/Facultystaff/hass/oc2web/lab/exp/qa/class/jones.pdf

Thanks!
Reply 3
Don't get too bogged down in the mechanism, it basiclly is analogous to Potassium dichromate. In this case - Yellow/orange to green.

remember the other standard tests

2,4DNP - orange ppt for aldehydes and ketones
Tollens (Ammononical silver nitrate) - silver mirror - Aldehydes

Im desperatelt trying to keep sharp - havent done this for months.
Reply 4
Sorry to bump this thread, but doesn't the reaction between phenols and FeCl3 involve a complex ion formation in which 6 phenol molecules combine with a Fe 3+ ion?

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