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By equation show the mechanism of the following reaction:
nucleophilic substitution reaction
Step by step
Solved in 2 steps
- Why aldehydes and ketones do not undergo nucleophilic substitution reaction?51Which of the following is not true about the mechanism for electrophilic aromatic substitution? O The carbocation intermediate has an sp3 carbon in the ring. O Benzene acts as a nucleophile. O The addition product is often a minor product. O Formation of a carbocation intermediate is the rate-determining step. O Aromaticity is regained by loss of H*.
- The Wittig sequence includes this/these reaction step/s. O nucleophilic substitution of a phosphine on an alkyl halide O acid-base reaction removing a hydrogen from the carbon next to the phosphonium group to form an ylide O the aldehyde or ketone combines with the ylide to form an oxaphosphetane O the oxaphosphetane breaks down to form the alkene and a phosphine oxide O all of the above O none of the above3-Hexanone can be synthesized from butanal and ethane using a Grignard reaction. The first step must be O creation of a carbocation O protonation of an oxygen nucleophilic attack of the aldehyde free radical halogenation preparation of an acetylideHelp please explain how to do both please.
- Which of the following would be a better starting material for a nucleophilic aromatic substitution reaction? Explain your choice using structures. Then provide the complete arrow pushing mechanism for the reaction of the better starting material and excess ethanol. CI CI O₂N NO₂ NO₂ NO₂• Same reagents as acid-catalyzed dehydration, except starting with a instead of an alcohol. • Same as the general mechanism hydrohalogenation, except with . Remember that EVERY acid-cat. mechanism begins with General Reaction: EXAMPLE: Provide H₂O H₂SO4 EXAMPLE: Provide the mechanism for the following addition reaction. H₂O H₂SO4 OH WH H₂O H₂SO4 as the nucleophile and ends with do PRACTICE: Provide the mechanism and predict the product of the following reaction. MAXOPredict the organic products, in any order, when the following alkene is subjected to ozonolysis with reductive work-up.
