Enter the numbers for the
mechanism arrows for the SN2 reaction.
Enter the numbers for the mechanism arrows for the SN2 reaction. - 1 2 H- 3 O 4 5 6 H2CH2CH2CH2C- 7 Br 8 H3CH2CH2CH2COH...
Enter the numbers for the mechanism arrows for the SN2 reaction. 8 12 9 H O 4 5 6 + H3CH2CH2CH2C- 7 Br H3CH2CH2CH2C- OH +
7. Add the curved arrows in the following reaction mechanism: Br, H +8 -8 Br-Br--FeBr3
raw the apropriate arrows (reversible, irreversible, no reaction) for the following reactions. (4 pts) Br +Br a) -C-o b) 7. Provide a curved arrow mechanism and predict the product for the following SN2 reactions. (9 pts) Br H2N a) b) C NachN Cl c)
8. The reaction of bromide 1 may proceed via an Sp2 mechanism. For this Sn2 mechanism, you may assume that the final deprotonation step (step 2) to form 2 is fast. CH3 on con CH; Br + H2O OH + H-Br + Br 1 (step 1) 12 + H OH + H-Br fast (step 2) a) What is most likely rate-determining step for this Sn2 mechanism? b) Please write the expected rate law for this Sn2 mechanism. c) Please draw...
30. Late papers not accepted. Work Independently. 1. Predict the most likely reaction mechanism (SN1, SN2, E1, E2) and draw all products. CH₂ Na O=CH₂ Hic Br 2 Draw complete mechanism with arrows for the SNI/E1 mechanism. Check for carbocation rearrangements CH3 + H2O 3. Which is the major product for the following reaction? Y CH + NaOH CH HO HO H₃ CH₂ H₃ HOCH CH₂ H₃ CHE CH₂ CH₂ CH3 CH 4. Name the following including the R/S, E/Z...
For the chemical reaction answer the following questions:
1. Is the mechanism Sn1 or Sn2?
2. What kind of substrate reacts in the following reaction? (2 °
, 2 ° allylic , 3 ° )
3. Is the role of the alkyl halide reactant an acid, base,
electrophile, nucleophile , or both a nucleophile and base?
4. Is the role of the reagent KI an acid, base, electrophile,
nucleophile , or both a nucleophile and base?
5. What is the...
7-11 pls
What reaction happens? SN1/SN2/E1/E2 And what are the products? Br Br NaCl DMSO ? NaOH 7. 1. Br NaOH Br NaOMe 2 8 3. t-BuOK Br NaOMe 9. Br Br ? ? DBN NaOH 4 10. Br NaOEt ? ? -BUOK 5. 11. NaSH
2. Draw a mechanism for the following SN2 reaction? [3] Br Cos SH NaSH + NaBr +
Predict the most likely reaction mechanism (SN1, SN2, E1, E2) and draw all products. Nato=CH₂ E2 ran Br major 2. Draw complete mechanism with arrows for the SN1/E1 mechanism. Check for carbocation rearrangements. CH3 SMI 애 + H₂O7
7) Give the mechanism including the transition state. сн.ct çı SN2 НН 8) Give the mechanism. CH1 보 SN1 CHCH,CH-C CH. но H Br 9) Give the mechanism of the reaction shown below. CH CI E1 CH,OH 10) When 1-bromo-2,2-dimethylcyclopentane is heated in ethanol, one of the products which results is shown below. Provide a detailed, stepwise mechanism for the production of this compound, and give the name of the mechanism by which it is produced. CH3 CH3