Sir as there is time left for the exam please make more videos like this. I just love how you style your videos and your explanation is amazing. Please make videos about organic chemistry A levels such as hard subjects like amines in A2, condensation polymers. You can even focus on the required practicals and what we need to know for each if u want. I just want to thank you SO MUCH for your hardwork and the amount of time you put in this videos. I am for sure going to recommend you to other people. Thank U!!!
I really appreciate the kind words Shayna :) I will try, but I'm not a teacher and really limited with time atm so trying to focus more on the topic analysis videos. We will see though 😉
You're honestly a savour, my paper 2 is tomorrow and I'm speeding through your videos. I've never understood this before and struggled with remembering all the required mechanisms. I actually feel like I have a chance to pass now. Thank you
thank you so much for these videos! ive been going through all of your videos during this last week of revison for paper 1 :) if you can, please make more videos on electrochemistry because i never get marks on any of those questions,, again ty!!!!
I have a couple electrode potential/electrochemistry vids on the channel, have u checked them out? if so, is there anything you struggle with specifically? It's a heavy redox knowledge topic tbh
Hello! At 27:31, for question 4, can we say "Carboxylic acids and alcohols contain hydrogen bonding, whereas esters contain dipole-dipole forces. Hydrogen bonds are stronger than dipole-dipole forces. Therefore, it requires more energy to break the hydrogen bonds. Hence, esters have lower b.p" ?. Great video!
This a great video - nice visuals and very understandable explanation. Keep up the good work! Just a quick question - you said that esters can react with water to form a carboxylic acid and alcohol in the reversible reaction but when saying they're used for perfumes, you then said they don't react with water? Can you explain this please as I don't understand? I'd appreciate it a lot! Thanks again for the video - very simply explained with the perfect amount of detail! :)
Sure, I plan to :) Are there any topics you struggle with specifically? It is quite difficult with the copyrighting exam board have put on their content, but I will try my best
There aren't really any purely esters questions tbh, and if there are they're simple so I don't think it will be that helpful. It's mainly joint with other aspects of carboxylic acids topic like acyl chlorides and acid anhydrides etc.
This video is amazing! Just a bit of criticism though, you forgot to mention that carboxylate salts are used in soap, which is something you need to know (its in the spec)!!!
for hydrolysis in acidic conditions, H2SO4 is fine instead of HCl, but it MUST be dilute, not conc. :) you can read up more about it on chemrevise or chemguide if u want www.chemguide.co.uk/organicprops/esters/hydrolysis.html
just released one today on every transition metal ligand substitution, plus some extra info :) hopefully that helps. Will do my best to release more before paper 1. There are also multiple past paper transition metal question walkthroughs
@@easymodeexams33 Thank you sir, also I have been getting questions wrong for the electrode potentials and cells topic. I'm not sure if my knowledge is lacking, could you also do a video on that and on bonding topic ?
that isn't under this section of the specification, it is under acyl chlorides and acid anhydrides, I have made a video on those reactions and mechanisms
Get 1-1 Tuition with me: bit.ly/3YvshDh
MOST AFFORDABLE Chemistry Tuition (£10 per lesson!): bit.ly/3A5PoL1
Sir as there is time left for the exam please make more videos like this. I just love how you style your videos and your explanation is amazing. Please make videos about organic chemistry A levels such as hard subjects like amines in A2, condensation polymers. You can even focus on the required practicals and what we need to know for each if u want. I just want to thank you SO MUCH for your hardwork and the amount of time you put in this videos. I am for sure going to recommend you to other people. Thank U!!!
I really appreciate the kind words Shayna :) I will try, but I'm not a teacher and really limited with time atm so trying to focus more on the topic analysis videos. We will see though 😉
You're honestly a savour, my paper 2 is tomorrow and I'm speeding through your videos. I've never understood this before and struggled with remembering all the required mechanisms. I actually feel like I have a chance to pass now. Thank you
Good luck :)
ur a life saver thank you so much man
This guy is godly
I love this channel! Thank you so much for your work!
Thnx :) no worries, good luck!
thank you so much for these videos! ive been going through all of your videos during this last week of revison for paper 1 :) if you can, please make more videos on electrochemistry because i never get marks on any of those questions,, again ty!!!!
I have a couple electrode potential/electrochemistry vids on the channel, have u checked them out? if so, is there anything you struggle with specifically? It's a heavy redox knowledge topic tbh
Thank you so much for your videos, they're so helpful! I hope you gain more subscribers because you really deserve it, thank you so much
I'm glad you find them helpful, thnx for your kind comment :)
THANK YOU SO MUCH
Hello! At 27:31, for question 4, can we say "Carboxylic acids and alcohols contain hydrogen bonding, whereas esters contain dipole-dipole forces. Hydrogen bonds are stronger than dipole-dipole forces. Therefore, it requires more energy to break the hydrogen bonds. Hence, esters have lower b.p" ?. Great video!
This guy is the GOAT🐐
thanks u actual legend appreciate u! last exam today hopefully goes well :)
I hope it did go well :)
Thanks for the video I really like what you've done with your channel.
thanks :)
This a great video - nice visuals and very understandable explanation. Keep up the good work! Just a quick question - you said that esters can react with water to form a carboxylic acid and alcohol in the reversible reaction but when saying they're used for perfumes, you then said they don't react with water? Can you explain this please as I don't understand? I'd appreciate it a lot! Thanks again for the video - very simply explained with the perfect amount of detail! :)
could you do more exam walkthroughs please? you explain very well
Sure, I plan to :) Are there any topics you struggle with specifically? It is quite difficult with the copyrighting exam board have put on their content, but I will try my best
Hi. Great video as always. Could you do an AQA walkthrough on an esters question if possible please? Thanks :)
There aren't really any purely esters questions tbh, and if there are they're simple so I don't think it will be that helpful. It's mainly joint with other aspects of carboxylic acids topic like acyl chlorides and acid anhydrides etc.
@@easymodeexams33 fair enough. Thanks man
Could make videos on graph skills and interpretation,please?
Thank you so much this was super useful
happy to help :)
This video is amazing! Just a bit of criticism though, you forgot to mention that carboxylate salts are used in soap, which is something you need to know (its in the spec)!!!
Good point, thanks! This was my bad, I may remake this video when I have time. good luck!
Very helpful, thanks alot
no worries, good luck!
i thought because acid catalyst you need to make esters is conc h2so4 hence the hydrolysis process should also need conc h2so4. am i wrong?
for hydrolysis in acidic conditions, H2SO4 is fine instead of HCl, but it MUST be dilute, not conc. :) you can read up more about it on chemrevise or chemguide if u want www.chemguide.co.uk/organicprops/esters/hydrolysis.html
During esterification, isnt it that the OH comes from the carboxylic acid and just the H from the alcohol?
Thank you
could you do one video explaining transition metal? struggling to understand it.
just released one today on every transition metal ligand substitution, plus some extra info :) hopefully that helps. Will do my best to release more before paper 1. There are also multiple past paper transition metal question walkthroughs
@@easymodeexams33 Thank you sir, also I have been getting questions wrong for the electrode potentials and cells topic. I'm not sure if my knowledge is lacking, could you also do a video on that and on bonding topic ?
make a video on polymerisation please!!
why was he laughing at 20:20 loooooooool
How come you didn’t include the reaction between acid anhydrides and alcohols to form esters ?
that isn't under this section of the specification, it is under acyl chlorides and acid anhydrides, I have made a video on those reactions and mechanisms
chill with the adds
youtube automatically puts them through the video, I've deleted a bunch