the weaker the base SN1 reaction and the stronger the base SN2 reaction and they are as follows
D. Substitution Reactions: Use your own nucleophile and Draw the product/s. a. Sn1 b. SN2
Chapter 9: Substitution and Elimination be the reactions as either SN1 or SN2, then draw the correct mechanism and hnal proud он H2O
I'm having trouble understanding when to use SN1 or SN2 (or both) 0 Sn1 - Sn2 Homework Indicate the mechanism by which each of the reactions occurs. (Snl, Sn2, both Snl and Sn2, or NR) Draw the final Product (s) of the reaction. Draht HI > 7 yet tha 3 Matt Hal > © (27 Xy+HBr > "OH + HBr
What substitution mechanism (Sn1, SN2, both, or neither) is expected for the following compound? Br What substitution mechanism (Sn1, SN2, both, or neither) is expected for the following reaction? -nucleophile attacks 12 - inversion of conf SCH
In the substitution reactions below, draw the major product in the box provided and indicate in the small box whether the reaction is SN1, SN2, or neither. Be sure to show all stereochemistry. If more than one enantiomer is produced, write "+Enant" in the box with the product. [10] Product SN1/SN2/Neither NaCN Br DMSO NaOEt EtOH Br NaOMe MeOH NaOH Expensive Acetonitrile CH,Br DMF Nat
What would the products of these substitution reactions be? M ? Part 3b. Substitution Reactions. (15 points total) In the boxes provided, label each of the following substitution reactions below as Snl or Sn2. Then draw the expected substitution product(s) for each reaction (5 pts each, 15 points total). OF Sn1 or Sn2? OH El tema sa ROH # # NaOH ort DMSO NaO o=s OSMO Noor B
Compare and contrast SN1, SN2, E1 and E2 reactions. What are some obvious similarities and differences between each reaction pathway? What are the requirements for each reaction to work? Discuss why SN2 is in direct competition with E2 while SN1 is in direct competition with the E1 reaction pathway. What is the rate expression for each? Which reactions are concerted? Which reactions are step-wise? Which reactions are stereospecific and what is the stereospecificity of each that are? How do the...
52.Which are the characteristics and factors that reactions? SN1: 3'alcehels,a altehels E3: laus factors that influence SN2, SN1, E2, E1, and ElcB s should be the major product and machanism of he reaction bertween a secondary alyl halide and an alkoxide? ow can one determine whether an alkyl halide wil roduce a single alkene upon elimination with strong base? tween a tertiary alkyl halide and water? 55.What is the mechanism of the reaction be 56. What change could be made...
(S)-3-Chlorooctane m DMSO S SN2 Factors Nucleophile Strength Leaving Group Solvent d) Cla . NaBrº DMSO Syl SN2 Factors Nucleophile Strength Leaving Group Solvent SN1 and SN2 Reactions 1. For each of the following reactions • Provide a complete detailed mechanism and predict the products. Indicate if the reaction proceeds via a Snl or Sn2 mechanism • Include the specific stereochemistry where appropriate.
which substitution and elimination reactions follows Zaitsev’s rule? SN1, E1, SN2, E2?
4. Sn1 reactions are unimolecular and Sn2 reactions are bimolecular. What does this mean? Write the generic rate laws for Sn1 and Sn2 reactions. Which reagents do the rates of Sn1 and Sn2 reactions depend on? 5. Consider tert-butylchloride and 2-chloropropane. Which of these compounds is more likely to react via an Sn1 mechanism? Which is more likely to reactive via an Sn2 mechanism? Explain your answer. 6. Rank the following compounds in order of increasing likelihood of undergoing substitution...