Preparation of Organometallic Reagents from Grignard Reagents - Grignard reagents may be used to prepare other organometallic reagents, for example, ethylmagnesium bromide reacts with cadmium chloride to yield diethylcadmium.
2CH3CH2MgCl + CdCl2 yields (CH3CH2)2Cd + 2MgCl2
Indicate the product of the following reactions and name the organometallic product.
(A) 4CH3MgCl + SiCl4 yields ?
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Propose a suitable mechanism - Propose a suitable mechanism for the formation of the mixed anhydride in the reaction indicated below:
C6H5CH2CO2H + (CF3CO)2O yields C6H5CH2C-O-CCF3 (also has an O double bonded to the third C with two single pairs of electrons on the O. the same is double bonded to the fourth C. the middle O also have two lone electron pairs) + CF3CO2H
Perkin and related reactions - There are numerous condensations that are closely related to the Perkin reaction. Among these are the aldol /3Badv/, and /A3a/, Knoevenagel, Claisen, and Dickmann condensations. What general class of compounds can be prepared using each of these well-known reactions?
Friedel-Crafts Acylation - I have a problem with Fiedel-Crafts reactions and I am not sure of the end results of the product. Could you please explain to me the attached question?
nucleophilic aromatic substitution - Show the intermediates including all the resonance hybrid structures for the pentyl anion, that are formed. What products would expect to form and in what ratio.
For some reason, I don't believe my reactions are done correctly. Could you please explain it to me the correct way? (please see the attachment)