That is why this analysis is widely used application note , example 1 , example 2 in lab classes and beyond. Sign up to join this community. The best answers are voted up and rise to the top. Stack Overflow for Teams — Collaborate and share knowledge with a private group. Create a free Team What is Teams? Learn more.
Asked 4 years, 7 months ago. Active 4 years, 7 months ago. Viewed 17k times. In organic chemistry, the symbol R is used to represent hydrocarbon groups or hydrogen in a formula when you don't want to talk about specific compounds.
If you use the symbol more than once in a formula as here , the various groups are written as R 1 , R 2 , etc. In this particular case, the double bond is surrounded by four such groups, and these can be any combination of same or different - so they could be 2 hydrogens, a methyl and an ethyl, or 1 hydrogen and 3 methyls, or 1 hydrogen and 1 methyl and 1 ethyl and 1 propyl, or any other combination you can think of.
The acidified potassium manganate VII solution oxidises the alkene by breaking the carbon-carbon double bond and replacing it with two carbon-oxygen double bonds. Carbonyl compounds can also react with potassium manganate VII , but how they react depends on what is attached to the carbon-oxygen double bond. So we need to work through all the possible combinations. Warning: The rest of this page is going to look quite difficult, because it talks in some detail about compounds you probably won't have studied yet.
It may be best just to go through this quickly for now, and then come back to it later on after you have studied aldehydes and ketones. Carbonyl compounds which have two hydrocarbon groups attached to the carbonyl group are called ketones. Ketones aren't that easy to oxidise, and so there is no further action.
But see note in red below. If the groups attached either side of the original carbon-carbon double bond were the same, then you would end up with a single ketone. If they were different, then you would end up with a mixture of two. In this case, you would end up with two identical molecules called propanone. On the other hand, if one of the methyl groups in the original molecule was replaced by an ethyl group, you would get a mixture of two different ketones - propanone and butanone.
What would you get if there was a methyl and an ethyl group on both sides of the original carbon-carbon double bond? Again, you would get a single ketone formed - in this case, butanone. If you aren't sure about this, draw the structures and see. Important: This last section is a gross over-simplification for the purposes of the CIE A level syllabus.
In practice, ketones are oxidised by potassium manganate VII solution under these conditions. The reaction is untidy and results in breaking carbon-carbon bonds either side of the carbonyl group. If you are doing CIE, then you will have to learn this as stated above. If you are doing anything else, you probably shouldn't be wasting your time reading this anyway. Potassium manganate VII is such a devastating oxidising agent that it is rarely used in organic chemistry. Check your syllabus!
In this case, the first product molecule has a methyl group and a hydrogen attached to the carbonyl group. This is a different sort of compound known as an aldehyde. Aldehydes are readily oxidised to give carboxylic acids, containing the -COOH group. Why is KMnO4 a self indicator? What is the indicator used in KMnO4 titration? Why h2so4 is used in titration of KMnO4? Why does KMnO4 turn pink? Why does KMnO4 changes Colour?
What is KMnO4 used for? Medical uses. Can K2Cr2O7 oxidise alkene? What is the purpose of acidifying a solution? Can I drink potassium permanganate? Is potassium permanganate good for skin? What can KMnO4 oxidize? What is baeyer reagent? Is KMnO4 polar or nonpolar? How do we prepare potassium permanganate solution? What is end point in titration? For it to be so it needs to be reduced, I. It needs to gain electrons.
For the most part oxygen almost always does this however, if it gets bonded to a much more electro negative atom such as fluorine then oxygen becomes oxidised and the fluorine reduced. What is a good oxidizing agent? This means that they easily attract electrons. As you can see in the periodic table of elements, the halogens that are good oxidizing agents are fluorine, chlorine, bromine and iodine, with fluorine being the strongest oxidizing agent among the four, followed by chlorine, bromine and iodine.
What does titration mean? A titration is a technique where a solution of known concentration is used to determine the concentration of an unknown solution. Typically, the titrant the know solution is added from a buret to a known quantity of the analyte the unknown solution until the reaction is complete. Why is k2cr2o7 not self indicator? Potassium dichromate acts as oxidizing agent in acidic medium only. Thus an indicator is must in this titration.
Why h2so4 is added in titration of KMnO4?
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