Q: Which of the following compounds is the most basic? A. p-methoxyaniline B. aniline C.…
A: As we know that aromatic amines are less basic than the alipahatic amine , because of resonance…
Q: Explain the reactivity and orientation effects observed in each heterocycle.a. Pyridine is less…
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Q: Explain why protonating aniline has a dramatic effect on the compound’s UV spectrum, whereas…
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Q: Describe how an electron donating group on an aromatic ring affects the proton chemical shifts of…
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Q: HNO3 `NH `NH H2SO4 NO2 Acetanilide para-Nitroacetanilide
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Q: f. propanoic anhydride g. cyclohexyl propanoate h. 3-methylhexanoyl chloride i.…
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Q: Draw the rearrangement-elimination product of 2-ethyl-3-methyl-2-(1-methylethyl)butan-1-ol, sulfuric…
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Q: `NH HNO3 `NH H2SO4 NO2 Acetanilide para-Nitroacetanilide
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Q: Example #1: Predict the substitution pattern when this compound undergoes a sulfonation reaction. |…
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Q: Explain why benzaldehyde is less reactive than cyclohexanecarbaldehyde towards nucleophilic attack.
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Q: DMSO KOt-Bu KBr + major product & NaCl a = Electrophilic addition d = SN2 Nucleophilic substitution…
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A: According to the reaction mechanism option (f) carbonyl nucleophilic addition is correct answer.
Q: Name and Draw the structures of all possible chemical (Electrophilic aromatic substitution)…
A: Since we only answer up to 3 sub-parts, we’ll answer the first 3. Please resubmit the question and…
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Q: 8. The structures of pyrrole and pyrrolidine are shown in the box. NH NH рyrrole руrrolldine What is…
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Q: Which one is INCORRECT? a.Br2 : electrophilic aromatic substitution b.Neutral KMnO4 : oxidation…
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Q: Br NaOH heat Draw E1 Major Product + Draw Minor E1 Product
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Explain the reactivity order of the given de/activating groups:
- alkyl
- amide
- bromine
- hydroxyl
- methoxy
- phenoxy
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Solved in 2 steps
- Identify A-D18.04a5 Add curved arrow(s) to draw the final step of the mechanism. H₂O *-* CH3 H3C H3C H₂C H N CH3 Edit Drawing H₂C NO₂ CH3 CH3In the anhydride compounds, the Sym stretching of the carbonyl groups Higher than Asym stretching .A O Smaller than Asym stretching .B O No relation between them.c O Equal.D O
- Foro 5 Answer the following questions about activating and deactivating groups. Give specific examples. 1. What makes one activating group stronger than another activating group? 2. What makes one quenching group stronger than another quenching group?Explain why the reaction in Problem 18.48 proceeds dramatically more slowly under neutral conditions than under either acidic or basic conditions.Identify the leaving group for a potential elimination of the following compounds. Compare the leaving group activities for A and K. Which of the following compounds cannot be subjected to elimination? Explain.
- In the following reaction, iodine monochloride (ICI) effectively serves as a source of an electrophilic lodonium species, l'U. Org. Chem 2005, 70, 3511-3517). Propose a mechanism for the formation of each of the two products, A and B. OMe Fr A MeO ICI OMe BDraw all the resonance forms for the sigma complexes corresponding to bromination ofaniline at the meta, and para positionsidentify D and E
- The double bond of an enamine (alkene + amine) is much more nucleophilic than a typical alkene double bond. Assuming that the nitrogen atom in an enamine is sp2hybridized, draw an orbital picture of an enamine, and explain why the double bond is electron-rich.The reaction of 3-methylhex-3-ene with HBr produces two stereoisomers. Draw the two-step mechanism, using good curved arrow notation. Identify the HOMO and LUMO in both steps and explain why two products are formed, along with the optical activity of the solution.22.65 When the following acid chloride is treated with AICI3, followed by HCl and Zn(Hg), a product is formed whose 'H NMR and IR spectra are shown here. Draw the product and propose a complete, detailed mechanism for the first of these two reactions. .CI 1. AICI3 2. HCI, Zn(Hg) 100 80- ? 60 40- * 20- 7 4 3 1 4500 4000 3500 3000 2500 2000 1500 1000 500 Chemical shift (ppm) Wavenumbers (cm-1)