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Which of the following alkyl halides reacts the fastest in an SN2 reaction? A) chloromethane B)...
please answer for me all questions 1-20 1) Identify the alkyl halide that reacts the fastest in a Sn2 reaction. A) chloromethane B) 2-chloro-2-methylpropane C) 2-chlorobutane D) 1-chlorobutane 2) Identify the alkyl halide that reacts the fastest in an SN 2 reaction. A) 1-bromopropane B) 1-fluoropropane C) 1-chloropropane D) 1-iodopropane 3) Which of the following alkyl halides gives the slowest SN2 reaction? A) CH3CH2C1 B) Ci CH3CCH2CH3 CH3 C) CH3CHCH2CH3 CH2 CH3CHCHCH3 C1 СН3 4) Which of the following alkyl...
11. Which of the following alkyl halides will undergo the fastest SN2 reaction? < <===- ய
2. Draw the bond-line structures of the following alkyl halides. Choose the compound that is mostly to undergo an S2 attack by a nucleophile in each of the following comparisons: a. chloromethane vs. 2-chloro-2-methylpropane (tert-butyl chloride) b. 2-chlorobutane vs. 1-chlorobutane c. l-chloro-2,2-dimethylpropane (neopentyl chloride) vs. l-chloropentane
1. Compare the reactivity of primary alkyl halides in part 1 (SN2) of this experiment to the reactivity of primary alkyl halides today. What conclusions, if any, can you make about the reactivity of these molecules under these different conditions? Use specific data to make your point. 2. Compare the reactivity of secondary alkyl halides in part 1 (SN2) of this experiment to the reactivity of secondary alkyl halides today. What conclusions, if any, can you make about the reactivity...
Which of the following alkyl halides undergoes the fastest SN2 reaction with sodium cyanide, NaCN? ID: A 10. Which ot the tollowing aakyi nauraes undergoes the tastest sNL reacuon wnun soarum cyaniue. Ra a. methyl iodide b. ethyl iodide c. 2-iodopropane d. tert-butyl iodide
Decide the mechanism by which the following alkyl halides will be converted to alcohols by the substitution of the nucleophile, OH-. R-X + OH- → R-OH + X- SN1 SN2 more information needed 2-chloro-2-methylpropane SN1 SN2 more information needed 1-bromobutane SN1 SN2 more information needed 2-chloro-3-methylbutane SN1 SN2 more information needed 3-chloro-3-ethylpentane
5. Rank the reactivity of the following alkyl halides (A-E) for an SN2 reaction from the fastest (1) to the slowest (5) and explain your ranking. (10 pts) H3C-Br Br Ci
15 Which of the following alkyl halides is most reactive in an SN2 reaction with Lil? H2 Br H,c Br CHs HyC a) I b) II c) III d) All three have equal reactivities
Reactivity of Alkyl Halides a. Which test was overall faster? Give a rationale for why that test is faster. Use one of the substrates to help you explain, drawing an energy diagram might help as well. b.For the AgNO3 test: Which substrate was fastest and which was slowest. Why? Draw a mechanism and energy diagram to help you explain these results. Data Table Test Tube # Reaction Time NaI test Reaction Time AgNo3 test 1 2-chlorobutane 00:03.25 No reaction 2...
Which of the following alkyl halides is likely to undergo rearrangement by a 1, 2- methyl shift? A) 3-bromo-3-methylpentane B) 2-chloro-3, 3-dimethylpentane C) 3-bromo-2, 3-dimethylpentane D) 2-iodo-2-methylpentane Which of the following alkyl halides is the worst substrate for the Sn2 reaction? A) Br B) Br C) Br D) Br In the mechanism for the reaction shown below, the first curved arrow moves from_ to Н. CH3CH2NH2 H3C + CH3 A) carbon (in CH3CH2NH2) to oxygen B) oxygen to nitrogen C)...