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Reaction of a sulfonitric mixture with
a) a terminal
b) a non-terminal alkyne
Step by step
Solved in 1 steps
- Draw the tautomer of this enol. Include all lone pairs. Ignore inorganic byproducts. :OH: :0: H3O+ Draw Tautomer8) Devise a synthesis for the following conversion. BrWhat acetylide anion and alkyl halide can be used to prepare each alkyne? Indicate all possibilities when more than one route will work.
- Select the incorrect statement A. Both (a) and (c) are incorrect B. Grignard reagents react with H,0 to form alcohols C. Grignard reagents are sources of carbon nucleophiles D. Grignard reagents react with H* to form the corresponding alkane E. Grignard reagents are formed by reacting R-X + Mg + diethyl etherExplain why pentane-2,4-dione forms two different alkylation products (Aor B) when the number of equivalents of base is increased from one totwo.What Wittig reagent and carbonyl compound are needed to prepare each alkene? When two routes are possible, indicate which route, if any, is preferred.
- Match each reagent to the product that it forms. Multiple reagents may form the same product. нох Reagent Reagents SOCI2, pyridine: C CISO2CH3, pyridine: E HCI: A PCI 3: A A) B) "It "ft "bl H₂O D) E) F) پہلے علی علیہethers can often be prepared by Sn2 reaction of an alkoxide and alkylhalides, which is a better reaction between methyl iodide and methyl oxide?58) Draw the product resulting from the following reaction. Indicate any relevant stereo chemistry. Eto EtOH
