R Run hard@thehsc Well-Known Member Joined Oct 7, 2021 Messages 784 Gender Male HSC 2022 May 15, 2022 #1 ^^^^ my teacher said it was - but not too sure about it!!!
Nezuko---- Member Joined May 18, 2020 Messages 49 Gender Male HSC 2022 May 15, 2022 #2 I believe, so, substitution reactions with Cl2 or Br2 utilise UV Light, correct me if I'm wrong.
R Run hard@thehsc Well-Known Member Joined Oct 7, 2021 Messages 784 Gender Male HSC 2022 May 15, 2022 #3 yeah they do - its because the reaction requires energy to overcome the Cl2 and Br2 bonds
someth1ng Retired Nov '14 Joined Sep 18, 2010 Messages 5,558 Location Adelaide, Australia Gender Male HSC 2012 Uni Grad 2021 May 16, 2022 #4 I'd argue that it's technically wrong to say UV catalysed because the UV is consumed in the reaction. It's more accurate to describe it as UV activated/mediated. Last edited: May 17, 2022
I'd argue that it's technically wrong to say UV catalysed because the UV is consumed in the reaction. It's more accurate to describe it as UV activated/mediated.
R Run hard@thehsc Well-Known Member Joined Oct 7, 2021 Messages 784 Gender Male HSC 2022 May 16, 2022 #5 @someth1ng yh I would agree with that - its just that my teacher confused everyone by saying its a catalyst
@someth1ng yh I would agree with that - its just that my teacher confused everyone by saying its a catalyst
E ekjchale#1 Active Member Joined Apr 4, 2022 Messages 118 Gender Male HSC 2022 May 16, 2022 #6 Run hard@thehsc said: @someth1ng yh I would agree with that - its just that my teacher confused everyone by saying its a catalyst Click to expand... Damn our teachers r similar then lol
Run hard@thehsc said: @someth1ng yh I would agree with that - its just that my teacher confused everyone by saying its a catalyst Click to expand... Damn our teachers r similar then lol