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Increasing alkyl substitution stabilizes an
inductive effect. Explain ?
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- How To Assign the Prefixes E and Z to an Alkene ? discuss by steps ?Please answer this Can you give examples to explain Addition reactions-general characteristics Benzene rings do not reactthi like alkenes Remember, the electrophile adds to the less substituted carbon, and the nucleophile to the more substituted carbon. Markovnikov’s Rule: The addition of a hydrogen halide to an alkene favors the product in which the proton adds to the alkene carbon that is initially bonded to the greater number of hydrogen atoms. Carbocation rearrangements- Methyl groups and hydride groups can migrate to make a more stable carbocation. A primary carbocation is less stable than a secondary carbocation, which is less stable than a tertiary carbocation. Addition of A Strong Bronsted Acid Hydrohalogenation HX addition to an alkene. Goes through a carbocation intermediate. The electrophile (H+) adds to the less substituted carbon, and the carbocation forms on the more substituted carbon. The nucleophile (X-) then adds to the more substituted carbocation.…Give a clear explanation handwritten answer..complete the following reaction with explanation
- 1. Illustrate and explain how the compound below can be used to produce different alkenes. C5. Draw the structures of A and B, and use the curved arrow formalism to show the Trensproduct is med bond making and bond breaking that occurs in the formation of A and B through the following series of reactions. Note: Sodium hydride (NaH) is a strong base. NaH A diethylether Use the curved arrow formalism to show the bond meli9. Provide IUPAC systematic names for each of the following compounds. a)
- Give a clear handwritten answer..complete the following reaction..choose the perfect arrow for given reactionCan you explain how an alkene bonds to a metal like in this compound using some orbital diagrams?a) Draw the arrow-pushing mechanism for the reaction of hydronium with ethanol. Include all lone pairs and non-zero formal charges. b) Draw the arrow-pushing mechanism for the reaction of NaNH₂ with chloroform. Include all lone pairs and non-zero formal charges. c) Draw the arrow-pushing mechanism for the reaction of sodium hydroxide with phenol. Include all lone pairs and non-zero formal charges. d) Are any of the above reactions reversible? Do any of them go to completion? Explain your answer.
- Are terminal alkynes considered weak or strong acids? Explain why...Rank the alkenes stability from most to least and explain whyBe sure to answer all parts. By taking into account electronegativity differences, draw the products formed by heterolysis of the carbon-heteroatom bond in the following molecule. Classify the organic reactive intermediate as a carbocation or a carbanion. Use a skeletal structure to draw the organic ion. Li draw structure .