Carbanion Stability

First

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I never have understood the orbital lobes or how they are drawn as overlapping. When I look at the actual lobe, I was assuming that is the region the bonding and nonbonding electrons with the associated atom resides. Then when my book talks about sigma, pi and overlapping bonds... that whole perception breaks down. If electric regions are overlapping, why don't we just draw them that way? I don't understand.

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On the first group methyl is the least stable, then it became the most stable for the second group. How's that so?

What is the relation of carbanion with stability??

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But aren't anions negatively charged?

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I totally forgot that the stability of carbanions is exactly opposite to that of carbocations. Thanks for reminding me, and thanks again for all of your wonderful videos!

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So here he compared carbocations with carbanions?

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