LiAlH[Ot-Bu]3 For The Reduction of Acid Halides To Aldehydes
Reduction of Acid Halides To Aldehydes With LiAlH(OtBu)3 or Rosenmund’s Catalyst Acid halides can be reduced to aldehydes through use of the bulky reducing agent
Read moreReduction of Acid Halides To Aldehydes With LiAlH(OtBu)3 or Rosenmund’s Catalyst Acid halides can be reduced to aldehydes through use of the bulky reducing agent
Read morePotassium tert-Butoxide (KOt-Bu) Is A Bulky Base In a blatant plug for the Reagent Guide and the Reagents App for iPhone, each Friday I profile a different reagent that
Read moreI love getting letters from people about their experiences with organic chemistry. I love it even more when they share some of the techniques and
Read moreOzonolysis of Alkenes and Alkynes Alkenes can undergo oxidative cleavage with ozone (O3) to give carbonyl compounds, cleaving the C=C bond The reaction generates an ozonide intermediate,
Read moreLove this quote, from Organic Chemistry 1 as a Second Language by David R. Klein (fuller review to come) on organic chemistry and memorization. You
Read moreThe Carbocation Intermediate That Connects The SN1, E1, And Alkene Addition Reactions Was going to include this in my last post but it was getting
Read moreThe Wittig Reaction: A Useful Method For Converting Aldehydes and Ketones To Alkenes Some time ago, we learned how to turn alkenes into carbonyls via
Read moreUnderstanding The 7 Key Factors That Stabilize Negative Charge (And Ultimately, Basicity) Like I wrote about in a previous post, (See article: Curved Arrows For
Read moreSodium Metal (Na) As A Reagent In Organic Chemistry In a blatant plug for the Reagent Guide and the Reagents App for iPhone, each Friday I profile a different
Read moreStabilization Of Positive Charge In Organic Chemistry: 7 Key Factors Just to clarify: make sure you’re familiar with how formal charge can mislead before you
Read more