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Q: cold KMN04 ??
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Q: Bonus: Propose a mechanism Must be perfect for any points NaOEt OEt EtO EtO HOE!
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Q: (b) Predict the products and depict the mechanism : coci
A: Answer is attached as follows
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Q: CI- Br Br Br 5. 6. HO 4.
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Q: DMSO T = 100°C 29. CH,O in CH,OH at 100 degrees C 30. Br 31. ONLY PRODUCT
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Q: Please show me the mechanism for O3+2-methyl-2-butene, stoping at the ozonide?
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Q: Propose a complete reaction mechanism for radical reaction of CH4 + Cl2.
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Q: 3) Write a detailed mechanism of: CH CH. HNOT H'SO NO
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Q: Provide the appropriate reagent(s) and conditions for the following transforma ベロで NH2 Ph Ph Ph Ph.
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Q: (v) Br2/CHC13 →?
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- (S)-2-Butanol, CH3CH2CHOHCH3, slowly racemizes on standing in dilute aqueous sulfuric acid. Explain, illustrating with a mechanism.Provide a reasonable mechanism for 1(b)Which reagent(s) sequence(s) is/are optimum for preparing butanoic acid from 1-propanol? i. K2Cr2O7 in acidii. (1) PBr3; (2) NaCN; (3) H2O; (4) [H+] iii. (1) NaCN; (2) H2O; (3) [H+]iv. LiAlH4
- Predict the mechanimsm and reactants to synthesize the picture below. Write legibly and ill give you a thumbs up.What are the groups towards meta position give examples and what its mechanism ?Describe the structure of the methylethium tetramer (including the orbitalsinvolved in the bonds) and indicate a reaction in which this compound isapplied.
- Use your knowledge of directing effects, along with the following data, to deduce the directions of the dipole moments in aniline and bromobenzene.The structures of two tertiary bicyclic chlorides (compounds 1 and 2) are shown below. Which of the following statements is correct?Show the curved-arrow mechanism for the first step, and the structure of the cyclic intermediate formed, when cyclopentene in treated with KMnO4 . A Lewis structure for the permanganate ion is provided in the hint. Make sure to show all non‑bonding electron pairs and formal charges where necessary. Omit K+ .
- One possible way of determining the identity of an alkene, is to let itundergo an oxidative cleavage reaction in the presence of hot basicpotassium permanganate. You are given two containers said to containdifferent alkenes. Container A is marked as cis / trans‐2‐butene andcontainer B as 2‐methyl‐1‐butene. Explain by referring to the formation ofproducts, how you would verify the identity of the alkenes.give reactions and intima mechanism of following reactions-Predict the major organic product formed when the compund shown below undergoes a reaction with H2O2 and then is heated in H2O. The 2nd photo is what I thought was the answer, but when I put it into Mastering Chemistry, it was counted as wrong and my feedback was, "What configuration is the C=C bond expected to haev?" I'm confused as to what this is referring to, so I appreciate any help given.