Wheel of No Grignard Reactions

The Grignard reagent is synthetically versatile as the organomagnesium compound can react with a variety of electrophiles.


The mechanism is not well-understood and most likely involves a single electron transfer (SET).

The reactions require dry solvents such as THF (Tetrahydrofuran).

Grignard reagents cannot be prepared using molecules having acidic hydrogens or electrophilic centers. Carbon dioxide or conjugated systems also react with Grignard reagents.



Wheel of no Grignard reactions: Click/tap to enlarge the image

For a whopping wheel of Grignard reactions, click HERE.

What other wheel(s) 🎡 of organic reactions would you like to see❓ Questions Let Chemaficionado know in the comments below or at mychemistryhomework@gmail.com

References:

(1)    Chouhan, M. S. Advanced Problems in Organic Chemistry for JEE, 11th Ed.

(2)    Ncert. Chemistry : Textbook for Class XII - Part.II; National Council Of Educational Research And Training: New Delhi.

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