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- Consider this nucleophilic substitution reaction. 1. Highlight the electrophilic carbon in red, and highlight the leaving group in blue. Highlight the atom in the nucleophile that will attack the electrophilic center in green. Only atoms need to be highlighted and not the lone pairs or formal charges. 2. Draw the product(s) of the reaction. Include all lone pairs.I'm looking for an alkene with a single methyl group and an anti markovnikov Br at the last carbon and the markovnikov with Br on the bottom. The image is attached is just to illustrate positioning of the Br, and not an actual alkeneDetermine the number of carbons present in the compound based on the base name. Draw the carbon chain and include any double or triple bonds if indicated in the suffix of the base name. Number each carbon. The carbons can be numbered from left to right or right to left. Draw any substituents on the corresponding carbon atom for which is indicated in the name. Refer to Figures 4 and 5 in the background for a visual representation of numbered carbons with corresponding substituents. Check that each carbon atom has a total of 4 bonds.
- Answer all of question 1 pls 1.i. Give two examples each of Unsymmetrical alkenes and reagents.ii. Give two examples of reactions of alkenes that result in Anti-Markonikov’s addition productsCompound 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-yneThe addition of a halogen to an alkene results in a ___________ with __________ addition. tertiary halide, syn geminal dihalide, anti vicinal dihalide, anti primary halide, syn 1,1,2,2-tetrahalide, syn
- Carbocations rearrange with some ease. An example of this is shown below. Indicate, with the corresponding arrows, how this process occurs. The carbocation 2 is more stable than 1, why is this? Explain it using (drawing) structures.Curved arrows, lone pairs, and formal charges are missing from the attached reactions. Add curved arrows for the forward reaction and add any needed lone pairs and formal charges10. Use Hammond's postulate to determine which alkene in each pair would be expected to form a carbocation faster in an electrophilic addition reaction. Choose which is the more reactive compound (in the box) for both pairs.
- 1 example of reaction for each of the types of organic reactions: substitution, elimination, addition, and rearrangement. Show:a. the overall reaction (reactants --> products)b. the reaction mechanism (indicate intermediate product)c. indicate which is the reactive species or intermediate in the reaction (radical? electrophile? nucleophile?)d. overall description of the reaction eg., radical substitution or SRHow many alkenes with different stability can be formed from the haloalkane in Figure 8Add curved arrows to the starting materials to show the flow of electrons in a reaction. Then draw the structure of the initially formed product(s). Do not draw subsequent product(s) that may form. Be sure to add nonbonding electrons and formal charges, where applicable.