d. OMe + AICS C₂H120 CH₂ Ja AICI AICI + HCI

Diethylcarbamazine synthesis and which name reaction

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6) Answering the following questions about aryl amines a) Draw the curved arrow mechanism for the following reaction shown ( NH₂ CI NO₂ NINH, NO₂ b) Explain using diagrams why the following reaction does not work and why the above reaction in part a does work (1 NaNH, NO₂ NO₂ NH₂

a) Put these three common types of carbonyl compound in order of decreasing reactivity         ester          amide          acid chloride           b) For the least reactive, show the interconversion to its other resonance form:         How does this electron delocalisation make it stable?         c) For the most reactive, draw the mechanism of its undergoing hydrolysis (reaction with H2O): Why makes this type of carbonyl so reactive to nucleophiles?

Please don't provide handwritten solution..... what is the product for this substitution reaction below

Draw the organic product of the Bronsted acid-base reaction between the compounds shown below. Include all lone pairs and charges as appropriate. Ignore any counterions. •H :F: :O: :O: H Na Ⓒ 0:0- H

Arrange the following molecules in increasing order of acidity. Base it only on their structural differences and explain how it is so.   1. Butanoic acid, Propionic acid, Propylamine, Butane

please explain