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Solved in 5 steps with 5 images
- Consider the following aromatic compounds a para-substituted compound?, the most reactive towards EAS? an ortho-substituted compound? does not react with RX, FeX3?i need help filling out the following SN2 reactions with appopiate reactants, products, or reagents,Consider the molecule: rate the priority functional groups from highest to lowest A. Alkyl chain B. Ketone C. Carbonyl D. Anhydride
- 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-ynePlease solve correctly: Optio for Q1. a.)2-hexyne b.)3-methyl-1-pentyne c.)3-hexyne d.)1-hexyne e.)4-methy-1-pentyne Q2) a.)Alkenes react with nucleophiles and bases. b.)Alkenes react with electrophiles. c.)In the reactions of alkenes, the p bond is not always broken. d.)Alkenes contain double bonds from two sp-hybridized carbon atoms.Use the Hammond postulate to explain why (CH3)2C = CH2 reacts faster than CH3CH = CH2 in electrophilic addition of HX.
- Name the major product of the reaction between (S)-2-bromohexane and KCH3COO. Be specific with the configuration.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?Explain Orientation Effects in Substituted Benzenes ?
- 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.What is the strongest IMF in pure 2-octanone? I know it is a ketone and has some polarity due to this, but the carbon chain so long, I wonder if london dispersion forces are stronger?Reactions that target the substituents on arenes can change their behavior in EAS reactions. Do not give handwriting solution.
