please help!!! are my answers right???
please help!!! are my answers right??? True Larger atoms are better nucleophiles due to polarizability. False...
Determine if each of the following statements is true or false 1 Larger atoms are better nucleophiles due to polarizability. 2 The identity of the nucleophile affects the rate of an SN1 reaction. 3 SN2 reactions proceed via frontside attack. 4 Bimolecular reactions tend to be stereoselective. 5 SN2 reactions invert all stereocenters in a haloalkane. 6 Cl-, OH-, and...
I Select ] I Select ] True False I Select J ▼ The identity of the nucleophile affects the rate of an SN1 reaction SN2 reactions proceed via frontside attack ▼ Bimolecular reactions tend to be stereoselective. Select ] SN2 reactions invert all stereocenters in a haloalkane Select] Cl-, OH-, and H- are good all leaving groups [ Select ] Good bases tend to be good nucleophiles Select ▼ Branching adjacent to a reacting carbon slows SN2 reactions due to...
Organic Chemistry: Vocabulary: i.) If we have a weakly basic nucleophile and a secondary haloalkane we’ll generally get _ mechanism(s). a. SN1 only b. SN2 c. E2 d. E1 only e. SN1 and E1 f. no reaction This mechanism will have ____ stereochemistry, a. predictable b. random due to the ____. a. planar intermediate b. backside attack transition state c. frontside attack transition state d. anti-periplanar transition state _____________________________________________________ ii.) Carbocation rearrangements will tend to form the __ stable intermediate....
please answer these questions 1: Which of the following is true for the reaction of (1R, 2R)-1-tert-butyl-1-fluoro-2-methylcyclohexane with potassium hydroxide? a: The product is (E)(6R)-1-tert-butyl-6-methyl-1-cyclohexene b: The product is (Z)(6R)-1-tert-butyl-6-methyl-1-cyclohexene c: The product is (Z)(6S)-1-tert-butyl-6-methyl-1-cyclohexene d: The product is (E)(6S)-1-tert-butyl-6-methyl-1-cyclohexene 2: Which of the following is not true for regioselective reactions? a: Generally, the selectivity lies to toward the Saytzeff product in elimination reactions. b: In a regioselective reaction, there is one product that predominates. c: The transition states of...
Total Marks 53 Q1. True / False 1. Tertiary hydrogen is more reactive than secondary hydrogen towards chlorination. 2. Tertiary alcohol is less reactive towards HX than secondary alcohol. 3. Loss of electron density by carbon is called reduction. 4. SN2 is a twostep reaction. 5. In SN2 the stereochemistry at C is not inverted. 6. Smaller activation energy makes the reaction slow. 7. Bulky substrate favors the rate of SN? reaction. 8. Neutral nucleophiles are more favorable for SN...
need help with the boxed bullet point. writing the chemical reaction scheme for the experiment. Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part I Pre-lab Assignment for Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part 1 1. From The Organic Chem Lab Survival Manual ( edition) by Zubrick • Review pages 201-204: Standard Reflux. • Review pages 127-140: Extraction • Review pages 164-189: Distillation, Simple Distillation. The Distillation Example, and The Distillation Mistake. 2. Read this...