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- 1. (f) Provide a name for each molecule (I narrowed it down to two subparts)Question: How many C-types do each of the following compounds have? Label them a, b,c ... And Circle the carbon type that would be the most downfield. Please answer all 4 parts of the question. Thank you!Re-draw each of the following making sure to include lone pairs and formal charges in each drawing
- Propose a curved-arrow mechanism for this reaction. Use curved arrows to show movement of electron pairs, and draw structures for all important reaction intermediates. Be sure to show all lone pairs and nonzero formal charges.Why do I number the substituents in this direction in the naming of these compounds? That is, how do we know whether to number the substituents clockwise or counterclockwise?Draw the line-angle structure of the following compounds if applicable. note: I need the answer immediately. I will send a good rate right away as well.
- Label All the functional groups present in the structures below (to the right). Note that you should choose the higher priority functional groups.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-ynewhere are the head arrows. Please give me the lone pairs as well. thank you