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- Item 2 Draw the organic products formed in each reaction. Consider both substitution and elimination products, if possible. Indicate the type of reaction that happened (SN1, SN2, E1, E2). Include stereochemistry and regiochemistry if relevant. For multiple products, identify which is the major and which is th]e minor product. a. b. C. d. e. H₂C 9H **** CH3 CH₂CH3 Br Br CH₂CH C6H5 Br -OC(CH3)3 OC(CH3)3 CH3CH₂OH TOH CH₂OHGl A. intermediate. alkyl halide is most likely to undergo the reaction mechanism which forms a carbocationA H2N. Figure 9: Multi-step reaction sequence
- ited Draw both resonance structures of the most stable carbocation intermediate in the reaction shown. od m... • You do not have to consider stereochemistry. . Do not include anionic counter-ions, e.g., I', in your answer. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom Separate resonance structures using the → symbol from the drop-down menu. ● CH4 + ? HBrUse the dropdown menu to indicate whether the rate of the reaction shown below will increase, decrease, or remain the same when the reaction conditions are changed to X or to Y or to Z (see below). NaN3 'N3 Br CH3CN X: Change the leaving group from Br to CI Y: Increase the concentration of haloalkane Z: Increase the concentration of NaN3 X: choose your answer.. ^ Y: choose your answer... V Z: choose your answer... choose your answer... Remain the same Nex Decrease IncreaseCircle the correct bolded word. a. Hydrogenation of an alkyne with palladium on carbon can / cannot be controlled to give an alkene. b. When a reaction becomes more exothermic, the transition state looks more like the substrate / product. C. Addition of two equivalents of HBr to an alkyne results in a vicinal / geminal dibromide. d. An SN2 reaction involves the collision of two alkyl halides to form a new carbon-carbon bond. True / False
- 11. Draw the mechanism and final product. Br-BrQuestion 4 4. Draw the final major product(s) for each multistep synthesis reaction. H3O* OMe H3PO4 Jones EtzNH reagent H30* 1. O3 NABH3CN PBr3 KOC(CH3)3 -OH 2. DMS NH3, H3O* Br KOC(CH3)3 1. ВНз РСС H30* 2. HаОг, ОН CH2CI2Use the dropdown menu to indicate whether the rate of the reaction shown below will increase, decrease, or remain the same when the reaction conditions are changed to X or to Y or to Z (see below). NaCN Br CN CH3CN X: Change the leaving group from Br to CI Y: Increase the concentration of haloalkane Z: Increase the concentration of NaCN X: choose your answer... Y: choose your answer... Z: choose your answer... >