What is the classification of this alkyl iodide? What is the classification of this amine? 03°
Alkyl Bromide Alkyl Bromide Classification Base Base Classification | % Reaction | % 1-Substituted | % 2-Substituted Yield Alkene Alkene Alkene 90 1.0 M The data above is from a paper published in 1956 in a chemistry journal. Answer the following questions based on the data: 1. Draw the mechanism to show how each alkene product is formed from the alkyl bromide and the base. 2. What does Zaitsev's rule say about double-bonds that are formed in an elimination reaction?...
OH The compand can be prepared with on alkyl iodide & a suitable nucleophile. Identify the alkyl iodide & nucleophile that you would use. For onionic nucleophile you don't need to draw Counterion,
A student observes a ppt formed when she adds sodium iodide/acetone to an alkyl chloride. The ppt she observes is: sodium iodide Csodium chloride alkyl iodide a complex of acetone and alkyl chloride
How would the rate change in a reaction if you went from using an alkyl iodide to using an alkyl bromide? Specifically in a SN2 displacement of an alkyl halide.
Highest boilinan Reacting wla primory a secondary amine, (CH3)₂NH alkyl halide will produce a (n): What I know @ Amide Its NOT @d'amine 6 l'amine © 3 amine & what I think 4 What is the major organic product obtained from the following reaction? 1) Li Ally 2) Hod "NH CH3 NCH 2 I know it is NOT NHCHE oft
How many alkene products can be formed when the alkyl iodide shown below undergoes E1 elimination? 9. How many alkene products can be formed when the alkyl iodide shown below undergoes El elimination? CH3 CH CH A) 1 B) 2 C) 3 D) 4 E) 5
How many distinct alkene products are possible when the alkyl iodide below undergoes E2 elimination?
8) A common method where one alkyl halide is converted to another alkyl halide is known as the Finkelstein reaction. In one example of this reaction, the reaction of an alkyl chloride with potassium iodide is generally carried out in acetone to maximize the amount of alkyl iodide that is formed. Why does the solvent increase the amount of alkyl iodide? (Hint: Potassium iodide is soluble in acetone, whereas potassium chloride is not) (5 points).
3. An alkyl halide is reacted with sodium iodide and sodium chloride in separate test tubes. The rate was the same in both experiments. Is this an Syl or an SN2 reaction? How would you know? 4. Why is sodium iodide used as a solution in acetone in these experiments instead of a solution in water? 5. Will the reaction below be Spl or Sn2? Show the mechanism.
8. Draw the structure of 5-amino-3-bromo-3-methyl-2-heptanol. Classify the alcohol, amine and alkyl halide present in this structu re as primary, secondary and tertiary (1+3 points)