Brilliant video! Just one question though... Does the bond angle around oxygen in phenol change when the lone pair on oxygen is delocalized into the aromatic ring?
what if you used only 1br2 and not 3br2 would you still get a white precipitate ? Also is it always the case that you get three substitutions when you reacts bromine and phenol like surely if you only reacted 1br2 you would only produce bromophenol
MaChemGuy would you still get a precipitate if you used 1br2? And can you please clarify for exams what we are meant to do ..ie: do we always assume that excess br2 is used because normally they just say “when bromine reacts with phenol” so from that how are we meant to know If it’s excess br2 or not ..the same thing applies for phenyl amine like is it sways the case that excess br2 is used and we get tru substitution
MaChemGuy and lastly , when a phenol reacts with Nitric acid why do we get two isomers ? Shouldn’t the same idea apply like it does for bromine that you get three substitution. If you use the idea of isomers than is it right to say that when bromine reacts with phenol , you also get 2 isomers
@@ahmadghaffar6758 - it is not that the benzene decolourises the bromine. The bromine becomes a bromide ion in the reaction, then attaching to the ring. In that reactive process and change, it loses the red colour.
Genuinely don't know what i would do without these videos right now, thank you!
Happy to help!
You've saved my chemistry grade, thank you
These videos help so much, thank yu
Why is there 3 br2 for phenols can it not stay as br2 and only hv 2 br on the phenol
The assumption here is that excess bromine is used.
2.23 Electrophilic* ?
Haha yeah, a little embarrassing he didn't check his own spelling when pointing out the spelling of the word!
@@ezmuffin9837 mate not embarrassing to make mistakes every now and again he teaches people for free whats a small spelling mistake
Brilliant video! Just one question though... Does the bond angle around oxygen in phenol change when the lone pair on oxygen is delocalized into the aromatic ring?
will we need to draw the mechanism for the reaction of phenol , e.g you said that br2 with phenol is electrophilic sub so do we need to draw it out ?
Not on the ocr a spec
Thank you so much!
what if you used only 1br2 and not 3br2 would you still get a white precipitate ? Also is it always the case that you get three substitutions when you reacts bromine and phenol like surely if you only reacted 1br2 you would only produce bromophenol
Ahmad Ghaffar You are correct in what you say, assumption is that excess bromine is reacted hence the tri-substitution
MaChemGuy would you still get a precipitate if you used 1br2? And can you please clarify for exams what we are meant to do ..ie: do we always assume that excess br2 is used because normally they just say “when bromine reacts with phenol” so from that how are we meant to know
If it’s excess br2 or not ..the same thing applies for phenyl amine like is it sways the case that excess br2 is used and we get tru substitution
MaChemGuy another thing sir ..can benzene decolorise bromine when a halogen carries is used ?
MaChemGuy and lastly , when a phenol reacts with Nitric acid why do we get two isomers ? Shouldn’t the same idea apply like it does for bromine that you get three substitution. If you use the idea of isomers than is it right to say that when bromine reacts with phenol , you also get 2 isomers
@@ahmadghaffar6758 - it is not that the benzene decolourises the bromine. The bromine becomes a bromide ion in the reaction, then attaching to the ring. In that reactive process and change, it loses the red colour.
Hi! Will you be finishing A2 chemistry if you haven't already? Really need your help at A2!
Hi. 3 years later and how did you do in Chemistry A-level?
@mr gg Hi.5 years later how did you do?