PLEASE DO THESE QUESTION
1: How many products are formed from the reaction of NaCN with 3-bromo-2,2-dimethylbutane?
a: two
b: four
c: three
d: one
2: How many products are formed from the substitution reaction of NaCN with 2-bromo-3-methylbutane?
a: two
b: three
c: four
d: one
3: Which of the following terms BEST describes the stereochemistry of an SN2 reaction?
a: Inversion
b: None of these
c: Racemization
d: Retention
4: Which of the following terms BEST describes the stereochemistry of an SN1 reaction?
a: Inversion
b: Retention
c; Racemization
d: None of these
5: How many products are formed from the substitution reaction of NaCN with 1-bromo-3-methylbutane?
a: one
b: three
c; two
d: four
1 :- Two
2:- One
3:- Inversion .
4:- Racemization
5:- One
PLEASE DO THESE QUESTION 1: How many products are formed from the reaction of NaCN with...
28. Which statement best describes the mechanism of the S2 reaction? (a) back-side attack with inversion of configuration (b) front-side attack with retention of configuration (c) front-side attack with inversion of configuration (d) front- and back-side attack with racemization (@) back-side attack with retention of configuration . Under Sn2 reaction conditions, what product will be formed in the nucleophilic substitution of bromine by methoxide in cis-1- bromo-4-methylcyclohexane? (a) axial, axial trans-1-methoxy-4-methylcyclohexane (b) equatorial, equatorial cis-1-methoxy-4-methylcyclohexane (©) equatorial, equatorial trans-1-methoxy-4-methylcyclohexane (d)...
Consider the substitution reaction that takes place when (R)-3-bromo-3-methylhexane is treated with methanol. What of the following would be true? A.) The reaction would take place only with inversion of configuration at the stereogenic center. B.) The reaction would take place only with retention of configuration at the stereogenic center. C.) The reaction would take place with racemization D.) No reaction would take place.
Question 11 (2.5 points) The following reaction proceeds with which of the following characteristics? 1. TsCI, PYR OH 2. NacN, acetone a) Elimination with inversion b) Substitution with retention c) Elimination with retention d) Substitution with inversion
1. 3-methyl-1-butene on reaction with H-Cl forms two products, namely 2-chloro-3- methylbutane (minor) and 2-chloro-2-methylbutane (major). Illustrate the mechanism for the formation of these two products. Use curved arrows to illustrate electron movement and all intermediates must be shown. 2. 3,3-dimethyl-1-butene on reaction with HBr forms two products, namely 3-bromo-2,2- dimethylbutane (minor) and 2-bromo-2,3-dimethylbutane (major). Illustrate the mechanism for the formation of these two products. Use curved arrows to illustrate electron movement and all intermediates must be shown. 3. Calculate...
1.1What is the major product formed upon radical bromination of (S)-3-methylhexane? Select the best response. Draw the full mechanism. A. (S)-3-bromo-3-methylhexane B. (R)-3-bromo-3-methylhexane C. A mixture of (R) and (S) 3-Bromo-3-methylhexane D. (3R)-1-bromo-3-methylhexane 1.2 What is the major product obtained from the reaction of 2-methyl-2-butene with hydrogen bromide in the presence of peroxides?Select the best response. Draw the mechanism. A. 2,3-dibromo-2-methylbutane B. 2-bromo-3-methylbutane C. 2-bromo-2-methylbutane D. (E)-1-bromo-2-methyl-2-butene 1.3 There are 4 major products formed upon treatment of (E)-3-methyl-2-hexene with HBr...
Keeping in mind stereochemistry, how many products are formed by the reaction of one equivalent of HBr with 2-methyl-1,3-cyclohexadiene?
please give correct answer to these 5 questions with
explanations, thankyou
What is the name of the product formed from the following Sn1 reaction? When a substitution reaction takes place at a stereocentre, which of the following statements is TRUE? VoH HI Select one: a. An SN2 reaction results in inversion of configuration only b. An SN 1 reaction results in inversion of configuration only c. An SN2 reaction results in racemisation only d. An SN2 reaction results in retention...
In the following reaction two major substitution products are
formed. What relationship do these two products have?
H14.34-Level 2 In the following reaction two major substitution products are formed. What relationship do these two products have? CI-S-CH3 OH MeOH OMe O A Diastereomers O B Enantiomers ° C Ameso compound is formed O D Constitutional isomers O E No relationship at all
3. for each of the following, choose the reaction that would proceed more rapidly and give an explanation for your choice: (a) iodomethane or bromomethane with aqueous KOH (b) iodomethane or iodoethane with aqueous KOH (c) methanol or bromomethane with Nal dissolved in acetone (d) 2-bromopropane or 1-bromopropane with Nal dissolved in acetone (e) 2-bromo-2-methylbutane or 2-bromo-3-methylbutane with ethanol (f) aqueous KBr or aqueous HBr with butanol (g) 2-chloro-3,3-dimethylbutane or 2-chloro-3-methylbutane with potassium tert- butoxide (h) 1:1 or 1:4 by...
can you give me the correct answers with
explanations?
7. Snl reactions usually proceed with athons a rectn equal amounts of inversion and retention at the center undergoing substitution. slightly more inversion than retention at the center undergoing substitution. ntly more retention then inversion at the center undergoing substitution. (D) (E) sligh complete inversion at the center undergoing substitution. complete retention at the center undergoing substitution How many distinct alkene products are possible when the alkyl bromide below undergoes E2...