1 page 2. Name these aromatic compounds properly. a) b) Br 4. Write in the reagents need to transform benzene into this product. Benzene -> 4. Write out all the steps in the mechanism of this electrophilic aromatic substitution reaction. Include all resonance contributors. Cl2 Benzene → chlorobenzene FeCl3 266 NA SEP 22 étv
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- They are Sn1 and Sn2 reactions Answer step by step with explanation Please answer correct i will give you upvote.Which of the dompounds is most basic and why?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.
- Consider the reaction: Draw out the two possible substitution reaction pathways (SN1 and SN2) and include all possible products. Include the structure of any intermediates and provide the curly arrow mechanisms required for both pathways. Using your answer to the above, justify which reaction pathway (SN1 or SN2) is more likely to occurRepeat 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.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.
- Please provide detailed steps as I am using this to study, along with explanations as to what you did on each stepProvide the mechanism of the redica reaction below (b)Several reagents and several organic structures are shown below. Construct a multistep synthetic route for the synthesis of acetylene from ethane by dragging the appropriate pieces into the bins. Note that each bin will hold only one item, and not every given reagent or structure will be used. (Stoichiometry is omitted.)