3. Rank the following in order by the rate in which they could participate in an SN1 reaction (“1" being the fastest and "5" being the slowest to react). CI CI B-
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- Help me please3. Rank the following in order by the rate in which they could participate in an SN1 reaction (“1" being the fastest and "5" being the slowest to react).3. Rank the following in order by the rate in which they could participate in an SN1 reaction ("“1" being the fastest and "5" being the slowest to react). CI
- 2. Which reaction will occur at a faster rate? Explain your answer. Rxn A Rxn, B Br₂ FeBr3 Br₂ FeBr39. Which SN1 reaction in each pair is faster? a) CI b) (CH3)3CCI + H2O > H2O (CH3)3CBR + H20 → CI H,O 206alcohol. A carbocation intermediate is central to which of these reaction types? (circle) E1 E2 SN1 SN2
- Rank the following from most reactive to least reactive in an SN1 reaction.Arrange the compounds below in order of increasing reactivity in a SN2 reaction. 1. (CH3)2СНCI 2. CH3CH2B1 3. CH3CH2C1 A) 1; 2; 3 В) 3;B 2; 1 C) 1; 3; 2 D) 2; 1; 3 E) 3; 1; 24. Which one of the following compounds will react faster by SN1? PhBr PhCH2Br PHCH= CHBr MezCBr Ph:CBr A E
- 5) Consider the two E2 reactions above. Br Br NaOH DMF heat NaOH DMF heat a. What are the major products for each reaction? b. What is the mechanism for each reaction? c. Which reaction would be faster and why? Use words like "transition-state, intermediate and/or reactant/product stability" in your justification. Draw the reaction coordinate diagram for both to assist in your explanation.2) Rank the following compounds in order of their reaction rates in an SN1 reaction with NaF with 1 being the fastest reaction and 5 being the slowest. OTs Br CI5. Classify the following molecules in order of decreasing rate of SN2 reactions: Ethyl Chloride, t-Butyl Chloride, Methyl Chloride and Propyl Chloride.