based on the reactivity of reagent conditions and the products are as follows
1. S.1 vs S.2 vs E1 vs E2 Show the mechanism and predict the MAJOR product(s)...
please explain why and how they are E2/SN2/SN1/E1 3. Draw a structural formula for the major organic product(s) of each reaction and specify the mechanism by which each product is formed (SNI, S2, El, or E2). • NaOH H20 CH,CH ON CH,CH OH CH ON CH,OH CH OH Na DMSO
Q. Predict mechanism type (SN1, E1, SN2, E2) for the following reactions. If more than one is possible, predict which mechanism is more likely and explain why. 5 - HI ح . 0H SNI KOCH2CH3 KOCHCH - I want to wors. NaOH, H2O, 100°C في NaCN ي . HO )..NC دا SN2
2. (1.5 pts) Label the following reagents as Good or Poor Nucleophiles AND as Strong or Weak Bases. OK Na SH 3. (1.5 pt) Predict the productts) of the following reactions, if there are multiple products indicate which, if any, is the major product. Be sure to clearly mark the stereochemistry of chiral carbon atoms and draw multiple products if there is more than one stereoisomer that forms. HCI MeOH H2SO H2 Pd/BaSO4 quinoline 4. (3 pt) For the following...
Circle the mechanism (SN2, SN1, E2, or E1) responsible for the formation of each product in this reaction. If the product cannot be formed in the reaction, circle "not a product". (2 pts) ГОН SN2 SN1 E2 E1 S N2 SN1 E2 E1 SN2 SN1 E2 E1 S2 Sn1 E2 E1 not a product not a product not a product not a product
10. 26. Predict the major product and mechanism (E1, E2, SN1, or SN2): КОССH), acetone Br Predict the result of reacting НЕг ROOR НBr
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
(8 pts) For each reaction, predict what mechanism will account for the major product(s) formed and write (SN1, SN2, E1, E2 or N.R.) in the boxes provided. Explanations or drawings are NOT required. 4. а. Н-о Br heat b. OTs NaOEt НOE с. NaCl OTs DMSO d. CI CHон
predict the mechanism (Sn1, Sn2, E1, E2) and major products for each reaction 8) NaOCHy CH,CHE CH,OH CH CH heat H,PO heat KOB HOIBU CHO CH, NaN. Br. H NaOCH CH3CH2OH heat dapted from Ruehl
(3 pt) For the following reactions: a) Label the substrate (1°, 2°, 3°), reagent (Good/Poor Nu, Strong/Weak Base) and solvent (protic, aprotic). b) Determine what mechanism will predominate (SN1, SN2, E1, or E2). c) Draw the product(s) you would expect to form, paying attention to regioselectivity and stereoselectivity. 4. (3 pt) For the following reactions: a) Label the substrate (1º, 2º, 3º), reagent (Good/Poor Nu, Strong/Weak Base) and solvent (protic, aprotic). b) Determine what mechanism will predominate (SN1, SN2, E1,...
E2 Reaction 2. Draw all constitutional isomers formed in each E2 reaction and predict the major product using the Zaitsev rule. Be OH El Reaction 3. What alkene is the major product formed from each alkyl halide in an El reaction? 4. Label the mechanism as SN2, SN1, E2 or El. You do not have to draw the product(s). CHO CH3-C-CH2-CH CH