Introduction to Rearrangement Reactions
Introduction to Rearrangement Reactions Reactions that involve a carbocation intermediate may be accompanied by rearrangements where a pair of electrons from a C-H or C-C bond
Read moreIntroduction to Rearrangement Reactions Reactions that involve a carbocation intermediate may be accompanied by rearrangements where a pair of electrons from a C-H or C-C bond
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 moreMaking Alkyl Halides From Alcohols In today’s post we show that treating alcohols with HCl, HBr, or HI (which all fall under the catch-all term
Read moreHydration of Alkenes to Give Alcohols When alkenes are treated with aqueous acid (H3O+) they can be converted to alcohols. Formation of the new C-OH
Read moreCarbocation Rearrangements In Alkene Addition Reactions In exploring reactions that proceed along the carbocation pathway, every once in awhile you might see an example of
Read moreAlkyl Shifts In Carbocation Rearrangement Reactions, Including Ring Expansion Hydride shifts can sometimes occur when a more stable carbocation can be formed through migration of
Read moreThe SN1 Reaction Mechanism There are two important classes of nucleophilic substitution mechanisms – the SN1 and SN2 mechanisms (See article – Two Types of
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 moreHow To Calculate Formal Charge To calculate the formal charge of an atom, we start by: evaluating the number of valence electrons (VE) the neutral
Read moreResonance Structures With Positive Charge: Four Key Principles As I mentioned before, the resonance form(s) of lowest energy are those where the charges are minimized.
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