what is the oxidation number of carbonyl carbon in CH3COO^-1?
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The first carbon in acetic acid, or CH3COOH, has an oxidation number of -3.
Here's how the Lewis structure for acetic acid looks like
Now, when you assign oxidation number, you have to keep in mind the fact that the more electronegative atom will take both the electrons from a bond in forms with a less electronegative atom.
When two atoms that have the same electronegativity are bonded, their oxidation numbers are zero, since no electrons are being exchanged between them (they are shared equally).
Now, if you look at the left carbon, you'll notice that it's bonded to three hydrogen atom, all less electronegative than carbon, and to another carbon atom, which has, of course, the same electronegativity (EN) value.
This means that carbon will take both the electrons from the bonds it has with hydrogen, leaving hydrogen with its classic +1 ON, and giving it a -3 ON.
By comparison, the carbon on the right will lose all the electrons it contributes to the bonds with oxygen because oxygen is more electronegativethan carbon.
As a result, the right carbon will have an ON of +3.
You can check your result by keeping in mind that the sum of the oxidation states for all the atoms must be, in this case, zero.
C2H+14O−22
ONC+4⋅(+1)+2⋅(−2)=0⇒ONC=4−4=0
This leaves carbon with an ON equal to zero, which is what you get if you add the oxidation states of each individual carbon atom
−3+3=0
Here's how the Lewis structure for acetic acid looks like
Now, when you assign oxidation number, you have to keep in mind the fact that the more electronegative atom will take both the electrons from a bond in forms with a less electronegative atom.
When two atoms that have the same electronegativity are bonded, their oxidation numbers are zero, since no electrons are being exchanged between them (they are shared equally).
Now, if you look at the left carbon, you'll notice that it's bonded to three hydrogen atom, all less electronegative than carbon, and to another carbon atom, which has, of course, the same electronegativity (EN) value.
This means that carbon will take both the electrons from the bonds it has with hydrogen, leaving hydrogen with its classic +1 ON, and giving it a -3 ON.
By comparison, the carbon on the right will lose all the electrons it contributes to the bonds with oxygen because oxygen is more electronegativethan carbon.
As a result, the right carbon will have an ON of +3.
You can check your result by keeping in mind that the sum of the oxidation states for all the atoms must be, in this case, zero.
C2H+14O−22
ONC+4⋅(+1)+2⋅(−2)=0⇒ONC=4−4=0
This leaves carbon with an ON equal to zero, which is what you get if you add the oxidation states of each individual carbon atom
−3+3=0
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the bayer villiger oxidation is the oxidative cleavage of a carbon carbon bond adjacent to a carbonyl which converts ketones to esters and cyclic ketones to lectons.
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