What are the possible resonance structures of CH_3-CH=CH-CH=OCH3CH=CHCH=O and CH_3-COO^-CH3COO? What is the order of stability of the contributing resonance structures?

2 Answers
Sep 17, 2015

See below.

Explanation:

Just remember that the electrons will move to the more electronegative atom or the more positive atom.

(a) But-2en-al

There is no positive atom, but "O"O is the most electronegative atom, so let's move electrons to the "O"O atom.

underbrace("CH"_3"CH=CHCH=O")_color(red)(bb "A") ⟷ underbrace("CH"_3"CH=CH"stackrelcolor (blue)(+)("C")"H-"stackrelcolor (blue)(-)("O"))_color(red)(bb "B")

Now the carbon atom has a + charge, so let's move electrons to it.

underbrace("CH"_3"CH=CH"stackrelcolor (blue)(+)("C")"H-"stackrelcolor (blue)(-)("O"))_color(red)(bb "B") → underbrace("CH"_3stackrelcolor (blue)(+)("C")"H-CH=CH-"stackrelcolor (blue)(-)"O")_color(red)(bb "C")

Structure bb "A" has the lowest energy and is the major contributor.

Structures bb "B" and bb "C" are higher in energy and are minor contributors.

(b) Acetate ion

Here again, there is no positive atom, but the other "O" atom is another electronegative atom.

Let's move the electrons toward it.

www.chem.ucla.edu

You can also move the electrons in the carbonyl group to the carbonyl "O" atom to get the third structure shown below.

resonance contributors
(from www.chem.ucla.edu)

Of the three structures above, the first two are equivalent and of equal energy.

The third structure is a minor contributor because it has three charges instead of one,

Jan 11, 2018

Although Ernest provided an attentive, helpful answer, I have provided the bond-line structures for the resonance structures, below.

For the first molecule, there aren't many resonance structures that adhere to the octet rule besides the one we start with,

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The electrons move to the right with each resonance structure. The first is major, and the rest our minor due to its octet rule satisfaction.

For acetate, I think Ernest did a fine job that doesn't need any more detail.