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There are many mechanisms in organic chemistry such as nucleophilic substitution, nucleophilic addition, elimination reaction, electrophilic substitution, etc. Elimination reactions involve elimination of any group. The dehydration of alcohol is also an example of elimination.
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Solved in 2 steps
- Give a clear explanation handwritten answer..complete the following reactionIdentify the electrophile and the nucleophile in each of the following reaction steps and then draw curved arrows to illustrate the bond-making and bondbreaking processes.Give a clear explanation handwritten answer..complete the following reaction with explanation
- Compare isoquinoline and quinoline..Explain their basicity.Which of them will be more susceptible to nucleophilic attack and electrophilic attack ? Explain the reason?Explain clearly Giving and example and mechanisms, explain the aromatic Substitution reactions.Explain the below ? Carbanions are nucleophiles
- If possible please answer all questions. Provide a complete, detailed curved-arrow mechanism for the following reaction. Include all lone pairs and formal charges. Using the mechanism and a few words,explain the why the NaOH deprotonates at the a-position and not the b-position or the aldehyde hydrogen. Also explain why the indicated alkene is formed in the 2nd second rather than the other possible alkene product.Which of the following statements about substituent effect in electrophilic aromatic substitution reactions (E.A.S.) is false? Electron-withdrawing groups (EWGs) passivates the benzene ring for ortho and para substitution Carbonyl group which are bonded directly to the ring are called electron withdrawing groups (EWGs) In nitration of benzaldehyde, major products are ortho and para-nitro benzaldehyde Regioselectivity in multiple subtitution is determined by the substituent which has a higher activation effect F, Cl, Br, and I are orto-para directing groups, but have passivating effectQ4. Nucleophilic attack at carbonyl with loss of carbonyl oxygen. For this question, answer AT LEAST FIVE of the SIX parts. (a) For the FOUR reactions listed below, draw structures of the major organic products. (i) (ii) (iii) HO OH ●... NMe₂NH₂ cat. dry HCI H Ph₂pⓇ THF
- Q1. Outline two methods of phenols synthesis. Q2. Give a concise account on the nomenclature of heterocyclic compound.Define central relationship between nucleophilicity and basicity in comparing two nucleophiles?Which compound(s) is (are) best suited for nucleophilic aromatic substitution reactions?