Problem 31 of 37 Submit Draw the product of the reaction below. Ignore inorganic byproducts. CH2OH OH HO OH OH Q excess CH³I Ag2O Draw Haworth Projection
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Q: IUPAC nomenclature for the compound?
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Q: Which of the following molecules is a cis alkene? oc OA A B OD OB 0
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Q: If an ideal gas has a pressure of 8.75 atm, a temperature of 467 K, and a volume of 60.31 L, how…
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Q: Claisen: OEt 1. NaOEt HOEt 2. H3O+ 1. NaOEt HOEt OEt EtO OEt 2. H3O+ EtO OEt
A: This is the mechanism for the 2 questions regarding the Claisen reaction You are welcome! Hope this…
Q: Provide IUPAC name for the structure shown below ОН O
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Q: What role does acid play in the Fisher esterification?
A: Fischer esterification is a chemical reaction used to synthesize esters. In this reaction, an…
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Q: 2. Propose and draw a reasonable mechanism for the following chemical transformation: O CH3OH, HCI,…
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Q: Show how you would perform the following synthesis, describing each step.
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Q: 16.126 Write the molecular formula for each of the following. (a) (b) (c)
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Q: Choose the best reagents to complete the following reactions.
A: 1) In this reaction, LDA in cold temperatures (to prevent self-condensation reactions) must be used…
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Q: Ita Srxn Substance HCOOH(aq) S (J-mol K-1) . 92.0 HCOOH(1) 128.95 H2C2O4(s) 115.6 H2C2O4(aq) 45.61…
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Q: ← Problem 23 of 37 Submit Draw the Fischer projection from the Haworth projection shown below. CH2OH…
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Q: Draw a plausible mechanism for the following transformation: 19.70a1 NH₂ N NH₂ [H₂SO] (-H₂O) X…
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- (a) What happens when CH3—O—CH<sub3 is heated with HI?(b) Explain mechanism for hydration of acid catalyzed ethene :CH2 = CH2 + HzO CH3—CH,—OHa. Propose a synthetic pathway for cis-[NiCl2(CO)2] using trans-effect. b. Propose the methods to differentiate the isomers in between [RhCl2(H2O)4]Cl and [RhCl3(H2O)3].H2O.The treatment of isoprene [CH2=C(CH3)CH=CH2] with one equivalent ofmCPBA forms A as the major product. A gives a molecular ion at 84 in itsmass spectrum, and peaks at 2850–3150 cm−1 in its IR spectrum. The 1HNMR spectrum of A is given below. What is the structure of A?
- In laboratory, Dr. Nur found out that the hydrolysis of nitriles (R—CN) when heated under reflux with dilute sulfuric acid yielded a major compound A. When compound A reacts with element N it showed that two products are produced (salt and gas). Meanwhile, the reaction of compound A with methanol yielded aromatic scent of compound B. She also noticed two products (compounds C and D) were obtained when she react compound B with reagent Lithium Aluminium Hydride (LiAlH4). Dr. Nur was observed compound C can be prepared naturally in the presence of enzymes in yeast through anaerobic conditions. Further investigation showed when compounds C and D can react with acidified potassium permanganate will produce compound (compounds E and F) with similar functional group. Dr. Nur also discovered compound E will produce silver mirror when react with reagent M and vice versa from compound F. Identify the possible expanded structure of compound A, B, C, D, E and F. Predict the…when H2O2 is added into acidified K2Cr2O7 which colour appears?Explain the following result. Acetic acid (CH3COOH), labeled at its OH oxygen with theuncommon 18O isotope (shown in red), was treated with aqueous base, and then the solution was acidified. Two products having the 18O label at different locations were formed.
- Why does the alpha hydrogen to a ketone have a lower pka value than the alpha h to an alkene. Draw a picture to explain ur a wayswhy the reaction of 2-bromopropane withNaOCOCH3 gives (CH3)2CHOCOCH3 exclusively as product, but the reactionof 2-bromopropane with NaOCH2CH3 gives a mixture of (CH3)2CHOCH2CH3(20%) and CH3CH=CH2 (80%)27. Which of the following reactions gives the product shown? Select all that apply.
- Explain the following result. Acetic acid (CH3COOH), labeled at its OH oxygen with theuncommon 18O isotope (shown in red), was treated with aqueous base, and then the solution was acidied. Two products having the 18O label at different locations were formed.Explain this result: Acetic acid (CH3COOH), labeled at its OH oxygen with the uncommon 18O isotope (shown in red), was treated with aqueous base, and then the solution was acidified. Two products having the 18O label at different locations were formed.Show how the synthetic scheme developed in Problem 23.67 can be modified to synthesize this triiodobenzoic acid X-ray contrast agent.
