Nucleophiles and Electrophiles
Nucleophiles and Electrophiles, Nucleophilicity and Electrophilicity All through the series on understanding where electrons are, and how they flow, we’ve been talking about how the
Read moreNucleophiles and Electrophiles, Nucleophilicity and Electrophilicity All through the series on understanding where electrons are, and how they flow, we’ve been talking about how the
Read moreI know I’ve said this before, but a whole lot of organic chemistry can be boiled down to “nucleophile attacks electrophile“. A nucleophile is a
Read moreAdding Acid Increases Leaving Group Ability Sure, it’s one thing to recognize halogens (Cl, Br, and I) as having high leaving group ability, as well
Read moreAn Introduction to Acid Base Reactions In Organic Chemistry Now that we’ve described how to figure out where the electrons are in a molecule, the
Read moreA few weeks ago I had the chance to interview (via e-mail) an instructor of organic chemistry at a medium-size American school, who shared her
Read moreFive Key Factors That Affect Acidity Today we’ll talk about five key factors that determine acidity for different molecules and a mnemonic (ARIO, or CARDIO)
Read moreBasicity In Organic Chemistry: Some Basicity Trends In this article we go through some important basicity trends in organic chemistry. (Previous article – Acidity Trends) The
Read moreThis time of year one of the most common problems students come to me with is how to do synthesis problems. Like this: There’s a
Read moreComparing the SN1 and SN2 Reactions In nucleophilic substitution reactions, a bond between carbon and a leaving group (C–LG) is broken, and a new bond
Read moreThe Acidity Constant Ka (And Its Negative Logarithm pKa ) Is An Extremely Useful Measure Of Acidity So last time we went through all the
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