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- Draw the organic product(s) of the following reaction. You do not have to consider stereochemistry. Include cationic counter-ions, e.g., Na+ in your answer, but draw them in their own sketcher. If no reaction occurs, draw the organic starting material. Separate multiple products using the + sign from the drop-down menu.Consider the following aromatic compounds a para-substituted compound?, the most reactive towards EAS? an ortho-substituted compound? does not react with RX, FeX3?Compound X is insoluble in cold KMnO4, Br2 in CCl4, and conc. H2SO4. Compound X is most likely: a. an alkane b. none of these c. an alkene d. an alcohol e. an alkyl halide Indicate which of the ff. statements regarding nucleophilicity is incorrect. F- is more nucleophilic, hence, more reactive towards methyl iodide than Cl-. Second row elements are more nucleophilic than first row elements of comparable basicity. The rate of SN2 reaction may be markedly affected by the nucleophilicity of the attacking atom. Nucleophilicity is the affinity of a nucleophile to an electrophilic carbon Which of the following alkynes can be deprotonated by NaNH2 in liquid NH3? 3-Methylhex-2-yne Pent-2-yne 3-Methylbutyne none of these Hex-3-yne
- PLEASE ASAP Major products for electrophilic addition transformations. Clearly show stereochemistry where appropriate (using wedged or dashed bond lines, or by writing axial or equatorial bonds). If no reaction is expected, write “NR”.Rank the following (in image one, the one with the chlorines) from most to least reactive in SN 1 reactions. How about ranking reactivity in nucleophilic addition (for example, Grignard) reactions in the second image?A hydrocarbon of unknown structure has the formula C8H10. On catalytichydrogenation over the Lindlar catalyst, 1 equivalent of H2 is absorbed. Onhydrogenation over a palladium catalyst, 3 equivalents of H2 are absorbed.(a) How rnany degrees of unsaturation are present in the unknown?(b) How many triple bonds are present?(c) How many double bonds are present?(d) How many rings ar e present?(e) Draw a structure that fits the data.
- You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. Do not include lone pairs in your answer. Draw phosphate groups, when present, as in the question: in basic form and with a phosphorous oxygen double bond.The above synthesis was designed using the Organic Chemistry Roadmaps in the appendix of your textbook. In this synthesis starting with acetylene, reagents from the table are used to carry out the indicated steps (shown in blue). In the box below, draw the structure of compound j. Use the wedge/hash bond tools to indicate stereochemistry where it exists. In cases where there is more than one answer, just draw one. Show stereochemistry in a meso compound. Do not include counter-ions, e.g., Na+, I-, in your answer.(10pts) Compound A, C10H16, was found to be optically active. On catalytic reduction over a palladium catalyst, 2 equivalents of hydrogen were absorbed, yielding compound B, CioH2o. On ozonolysis of A, two fragments were obtained. One fragment was identified as acetic acid (CHCOOH). The other fragment, compound C, was an optically active carboxylic acid, C8H14O2. Write reactions, and draw the correct structures for A-C, explain your answer in detail.
- Please indicate if it will also be an endo or exo product or both (50:50) and why. Thank you.A difficult problem in the synthesis of PGF2α is the introduction of the OH group at C15 in the desired conguration.a. Label this stereogenic center as R or S.b. A well known synthesis of PGF2α involves reaction of A with Zn(BH4)2, a metal hydride reagent similar in reactivity to NaBH4, to form two isomeric products, B and C. Draw their structures and indicate their stereochemical relationship.c. Suggest a reagent to convert A to the single stereoisomer X.Ignoring stereoisomers, draw the two possible enols for butan-2-one (CH3COCH2CH3), and predict which one is more stable.