Draw the complete, detailed mechanism for the reaction shown here, which produces an amidine-a nitrogen analog to an ester. H NH C=N 1. 2. CH,ОH Benzonitrile An amidine
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- Draw the complete, detailed mechanism and predict the products for the following reactions. HCN KCN, H2O (a) HCN NaOH, H20 (b)I would like to understand how to mechanism of this reactions occurAn imino chloride can be prepared from an amide according to the reaction shown here. Propose a mechanism for this reaction.
- Predict the product for the reaction between m-ethylbenzoyl chloride (see Problem 20.35) and each of the following. Draw the complete, detailed mechanism for each reaction. If no reaction is expected to occur, write “no reaction." (a) (CH3CH2)2CuLi; (b) LİAIH(O-t-Bu)3, – 78 °C; (c) NaBH4, EtOH; (d) C6H5MgBr (excess), then H*Provide a complete, detailed mechanism for the reaction CH;CH,OH shown here.Draw a plausible mechanism for the reaction shown below. Et Ме OH ..Me 1) Excess EtMgBr 2) Hо Et "CI
- Predict and identify the reactants of the following products. Draw the COMPLETE mechanism.No reaction occurs when benzaldehyde and propenenitrile (acrylonitrile) are combined. In the presence of a catalytic amount of NaCN, however, the reaction shown here takes place. Draw a complete, detailed mechanism to account for these results. Hint: See Problem 18.70. NaCN TH. + CN `CN HOH,0, ELOHConfused on how to continue with this mechanism reaction