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- Draw the products of the diethyl malonate: (1) sodium ethoxide; (2) isobutyl bromide; (3) HCl, H2O + ΔDraw the products and balance the equation.Draw the principal organic product for the reaction of 2-bromohexane with lithium in diethyl ether, followed by formaldehyde in diethyl ether, and then followed by dilute acid. Click and drag to start drawing a structure. X A G P
- 9. Draw the following chemical reactions. a) cyclopentylamine + water b) cyclopentylamine + butanoic acid c) cyclopentylamine + hydrochloric acid d) cyclopentylamine + benzoyl chloride e) cyclopentylamine + acetic anhydride17) which is not a vlable way to make a arboxylic acld functional grp? a) OH Hasou, HzO HaDoy, HaO i) O3 2 HQ i) x LAHBelow is one of the reactions used in the synthesis of lopinavir. What type of reaction is this? H -CI CI `NH3 N. но но Lopinavir NAOH, THE (solvent) O An SN2 reaction. O A hydrolysis. O Nucleophilic acyl substitution. O A nucleophilic addition.
- Draw the organic product you would expect to isolate from the nucleophilic substitution reaction between the molecules shown. Note: You do not need to draw any of the side products of the reaction, only the substitution product. D xx + H₂O + X Click and drag to start drawing a structure.Aspirin is an anti-inflammatory agent because it inhibits the conversion of arachidonic acid to prostaglandins by the transfer of its acetyl group (CH3CO−) to an OH group at the active site of an enzyme. This reaction, called transesterification, results in the conversion of one ester to another by a nucleophilic acyl substitution reaction. Draw a stepwise mechanism for the given transesterification.What is(are) the product(s) when benzoic anhydride is treated with the following reagent? + CH;CH,OH H. COH СОН benzamide COCH,CH3
