What To Expect In Organic Chemistry 2
Organic Chemistry 2 Is Largely About “Resonance” A large part of organic chemistry 1 is devoted to laying the foundations: introducing structural concepts such as
Read moreOrganic Chemistry 2 Is Largely About “Resonance” A large part of organic chemistry 1 is devoted to laying the foundations: introducing structural concepts such as
Read moreIf Org 2 has an overall theme, it’s “resonance”. Today’s post has a very simple message. Atoms with lone pairs, π bonds, radicals, and carbocations can
Read moreNucleophilic Acyl Substitution (With Negatively Charged Nucleophiles) Yes, there are a lot of reactions of carboxylic acid derivatives to learn! In this article we’ll explore
Read moreI don’t think there are that many “tricks” to doing well in organic chemistry, but there are a few. I was kind of surprised last
Read moreCarboxylic acids… are acids. I know that seems obvious. But it’s a near certainty that students taking Org 2 for the first time will forget
Read moreAbout a month or so ago I had a big revelation as an instructor. Something that I’d been taking for granted, that was right under
Read moreThe previous four posts on acid-base, substitution, addition, and elimination covered the 4 main reactions in organic chemistry I. Now it’s time to go beyond
Read moreQuestion: Are these molecules enantiomers, diastereomers, or the same? If you immediately recognized this as a molecule with an internal plane of symmetry (and thus
Read moreTry applying the rules for calculating oxidation states to carbon.
It’s going to feel a little bit weird. Why? Because there are two key differences.
First, carbon is often more electronegative (2.5) than some of the atoms it’s bound to (such as H, 2.2). So what do you do in this case?
Secondly, unlike metal-metal bonds, carbon-carbon bonds are ubiquitous. So how do you deal with them?
Drawing cyclohexane chair forms can be a tricky business. While it’s often intuitive to pick out which groups are up and down when they’re axial
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