Organometallics Are Strong Bases
Reactions of Grignard Reagents With Water, Carboxylic Acids, And Other Mildly Acidic Species Last post we talked about how to make certain organometallics, specifically Grignard
Read moreReactions of Grignard Reagents With Water, Carboxylic Acids, And Other Mildly Acidic Species Last post we talked about how to make certain organometallics, specifically Grignard
Read moreAll About The Reactions of Grignard Reagents Grignard reagents are excellent carbon-based nucleophiles as well as strong bases. They will add to aldehydes and ketones
Read moreUsing Protecting Groups In The Formation of Grignard Reagents Now that we’ve gone over the most useful reactions of Grignard reagents – addition to epoxides,
Read moreGrignard Practice Problems: Synthesis Exercises Involving Grignard Reagents Grignard reagents add once to aldehydes to give secondary alcohols and also add once to ketones to give tertiary
Read moreMore Grignard Practice Problems, This Time Incorporating Oxidation Here’s the summary for today’s post on synthesis incorporating Grignard reagents and oxidants. Converting an aldehyde into
Read moreHow Gilman Reagents (Organocuprates) Are Made Gilman reagents (organocuprates, often written as “R2CuLi” are not made the same way as Grignard or organolithium reagents. Instead of
Read moreSo What Are Gilman Reagents Used For, Anyway? Last time we talked about how to make Gilman reagents (organocuprates). In this post, we’ll talk about
Read moreTo my knowledge there are 8 different types of arrows you meet in organic chemistry. Here’s a little guide to them. 1. The forward arrow,
Read moreThe Heck, Suzuki, and Olefin Metathesis Reactions Are Really Cool. [But They Don’t Belong In (Most) Introductory Courses] There has been a trend in recent
Read moreWhat I Learned From A Massive Memorization Project This spring I had a weird obsession with birds. I ended up learning the names of all
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