Thermodynamic enolate - Study guides, Class notes & Summaries

1. Reaction of ethyl magnesium bromide with water will generate? a. ethanol b. ethane c. butane d. ethyl magnesium hydroxide e. a peroxide - b 2. Under conditions of thermodynamic control, product distribution is governed by: a. the relative stabilities of the products b. the relative energies of the transition states leading to the products c. the rate at which each product is formed d. a and b e. b and c - a 3. Which of the following statements is false for the reduction of camphor...

TAMU CHEM 238 FINAL EXAM QUESTIONS AND ANSWERS RATED A+ 1. Reaction of ethyl magnesium bromide with water will generate? a. ethanol b. ethane c. butane d. ethyl magnesium hydroxide e. a peroxide b 2. Under conditions of thermodynamic control, product distribution is governed by: a. the relative stabilities of the products b. the relative energies of the transition states leading to the products c. the rate at which each product is formed d. a and b e. b and c a 3. Which of the followi...

Tamu Chem 238 Final Exam Questions and Answers 100% Solved | Already Passed 1. Reaction of ethyl magnesium bromide with water will generate? a. ethanol b. ethane c. butane d. ethyl magnesium hydroxide e. a peroxide - b 2. Under conditions of thermodynamic control, product distribution is governed by: a. the relative stabilities of the products b. the relative energies of the transition states leading to the products c. the rate at which each product is formed d. a and b e. b and c ...

Different Nitrogen names - ANSWER Enamine: C=C-N Amine : C-N Imine: C=N Amide: O=C-N Imide: O=C-N-C=O Ketone(aldehyde) + 1° amine --> Imine Ketone(aldehyde) + 2° amine ---> Enamine think about it when replace the Oxygen of carbonyl and attach NitrogenR, /Make sure It has a lone pair. for the 2 ° amine move double bond to the C. Amine - ANSWER C-N Myopia (nearsighted) - ANSWER *(-)F= diverging mirror /convex mirror/concave lens *convex mirror: image always virtual...

This chapter contains all necessary information needed to know about the alpha carbon chemistry of carbonyl compounds. These notes are color coded. It contains information about acidity, enolization, alpha halogenation, aldol and claisen condensation reactions, malonic and acetoacetic ester synthesis, conjugate addition and michael addition reactions. Reactions and mechanisms are shown clearly with arrows, and explanations as necessary.