Exam 7: Organohalides: Nucleophilic Substitutions and Eliminations

Instructions: Consider the pair of reactions below to answer the following question(s). Refer to instructions. The nucleophile in these reactions is:

Instructions: Provide a IUPAC name for each of the following alkyl halides. Name: (Halothane)

Instructions: For each question, draw a structure corresponding to the given name. Draw: trans-1-sec-butyl-3-chlorocyclohexane

Instructions: Provide a IUPAC name for each of the following alkyl halides. Name: The solvents: CCl₄ and CH₂Cl₂

What is the rate law for the E2 reaction of an alkyl halide (RX) with sodium ethoxide (NaOEt) in ethanol solvent (EtOH)?

Which of the following represents the transition state of the S_N2 reaction between methyl iodide and ammonia?

Predict the product of the following reaction:

Instructions: Draw the structure of the major organic products(s) for each of the following reactions. Indicate the stereochemistry for each reaction when appropriate.

Instructions: Provide a IUPAC name for each of the following alkyl halides. Name: CHI₃ (iodoform)