IGCSE/GCSE/O & A Level/IB/University Student Forum
Qualification => Subject Doubts => GCE AS & A2 Level => Sciences => Topic started by: yasser37 on May 25, 2010, 08:53:57 am
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hi guys
What's the difference between using hot and cold KMnO4
for example in June 06 Q.4 Part f
thanks
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hi guys
What's the difference between using hot and cold KMnO4
for example in June 06 Q.4 Part f
thanks
hope this helped.. :)
if u still cant answer the question, tell me and i will help you ;)
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oh now I get it
thanks m8
will come up with more questions soon
hope to find you then
I finally got this
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oh now I get it
thanks m8
will come up with more questions soon
hope to find you then
I finally got this
ur welcome :)
dont worry ill be here ;)
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On that photocopy sheet... where u said with hot KMno4 will give a carboxylic acid or ketone....
do u mean that the CH2 will be removed and replaced by O (i know theres bond breaking/formings etc.. but for visual aid) and the double bond on the CH2 will also be replaced by a O... giving two carboxylic acids ??
... or just the double becomes a single and then forms a carboxylic and ketone...???
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On that photocopy sheet... where u said with hot KMno4 will give a carboxylic acid or ketone....
do u mean that the CH2 will be removed and replaced by O (i know theres bond breaking/formings etc.. but for visual aid) and the double bond on the CH2 will also be replaced by a O... giving two carboxylic acids ??
... or just the double becomes a single and then forms a carboxylic and ketone...???
if u still dont get it, just tell me i will try to explain it better if i can
sorry if i have bad handwriting ;D
hope it helped ;)
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oooh. right.. that makes sense.
thanks. !!!
ur writing looks like my bros... so im used to it. ;D
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if u still dont get it, just tell me i will try to explain it better if i can
sorry if i have bad handwriting ;D
hope it helped ;)
can u plz tell bout aldehyde
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What's wrong with aldehyde? If it's about oxidation, yes, it can be oxidised to carboxylic acid, Cr2O72-/H+
It can also undergo reduction using 3 methods, either LiAlH4, which is kept under dry ether because it is explosive, or you can reflux it with NaBH4 or you can react it with hydrogen and a Ni/Palladium catalyst. The product is usually primary alcohols
Anything else you want to know?