Which of the following reactions describes why AICI3 needs to stay dry in order for it to be used in a Freidel Crafts Acylation? A) 2 AIC13 + 6H2O → 2 Al(OH)3 (s) + 3 Cl2(g) + 6H2(g) B) AICI3 + 6H,O → [[Al(H2O);5 (OH)]+ H+ + 3 CI C) AICI3 +H2O → HAICI3* + OH¯ D) All the reactions, listed above, are competing for the Al³+ ion

H NH₂ ཡིནྣཾ ༥ ཨ ཨནྡྷ༥ ༠ ཨི་ཝཱ, ཙ ཨ་ར༩ H NH3+ the acidity of the amine ion drives the reaction to shift toward the conjugate base of the carboxylic acid product. the resulting carboxylic acid ion is a weaker base than an acetate ion. O aldehydes are more reactive toward nucleophiles than ketones. Onucleophilic attack occurs preferentially at the less hindered carbon of the formyl group.

Write the structure of the compound that will be produced in the following reaction?  CH3 –C ≡ C–CH2– CH2 – CH3     + 2HBr→

When propene reacts with gaseous hydrogen bromide, HBr, two products, 1-bromopropane and 2-bromopropane are formed. The reaction is a two-step process in which the electrophilic attack occurs in the first step. Identify the electrophile in this reaction Draw a diagram showing the first step of the reaction that leads to the production of 2-bromopropane.