CH3 Br2/FeBr3 C3H,BrO 6. C) Using resonance structures, justify whether the acetyl group of compound 5 will direct the bromination reaction to the meta or ortho/para positions.
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Part c
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Solved in 2 steps with 1 images
- Could someone help me with ranking these with how reactive they would be with an SN2 reaction? Thanks :)In parts 1 and 2 draw the two organic products of this reaction, showing any nonzero formal charges. Then, in part 3 answer the question regarding purification of the reaction mixture. 1. Draw the product with the higher molecular weight here: 2. Draw the product with the lower molecular weight here:the mechanism of halogenation of thiophene, when the halogen added to the position 2 and 3 , also provide the resonance structure and final product
- Identify the two most likely sites for an S2 reaction to take place in the molecule shown below.For SN1 Explain if 3o ( tertiary) alkyl halides reacted (fastest or slowest) explain why. Be sure to explain if alkyl halides did not react or did react and why. 3o (tertiary) compounds listed are: 2-chloro-2-methylpropane (see picture) Base your explanations on the following considerations: the nature of leaving group, the effect of structure, steric hindrance and any other feature.Assign the stereochemical configuration (E or Z) for the alkene below. Show your work, indicating clearly which groups are assigned high priority (e.g., through assigning the groups numbers, circling only the high priority groups, or labeling groups as high or low).
- Please help me with the organic chemistry problem below: Consider the reaction below: (Check the attached image) (it is between Furan and maleic anhydride, a DIels-Alder reaction) a) Will this reaction for an endo product (with a melting point of 80-81 degrees) or the exo product (with a melitng point of 114 degrees)? b) Carefully explain why the product must have been formed the way it did (exo or endo). c) Provide a mechanism for this reaction.1. State the effects of substituents on a benzene derivative towards further aromatic substitution. 2.Based on the above, suggest the various types of substituents that can be attached to Benzene.Is NaOCH2CH3 also a strong nucleophile? if so and Br wasn't a 3 degree alkyl halide, would it also undergo an Sn2 reaction? what would the major product be then?
- Order each of the following sets of compounds with respect to SN1 reactivity.Repeat Problem 14.36 for [8]annulene. Draw the π MO energy diagram for [10]annulene, similar to those in Figures 14-19 and 14-21. Fill up the orbitals with the appropriate number of π electrons. Based on this diagram, should [10]annulenebe aromatic or antiaromatic? Explain.Is the major product for 2-butanol and HCl racemic since its SN1?