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Q: Provide a name for each of the following molecules. -CEC-CH₂CH₂CH₂CH₂ SH OH Н HO 'H H OH SH
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Q: QUESTION 4 000 Arrange the following in order of increasing solubility in water: C₂H5OH; CO2; N₂O.…
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Q: In an experiment, it is found that the pH's of four salts, AA, AB, AC, and AD are 5.0, 6.5, 11.0 and…
A: Given: The pH values of AA, AB, AC and AD are 5.0, 6.5, 11.0 and 9.0 respectively.
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Q: Answer ALL parts of this question. Benzoic acid can be converted to the two products (A and B) shown…
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Q: Question 19.b of 23 Uranium hexafluoride, UF, is an important compound used in the enrichment of…
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Q: what is hydrogen addition of 40.0 m a. 0.0667 M b. 1.00 x 107 M c. 0.100 M d 150 x 10:13 M
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Q: Predict the splitting pattern for each signal in the ¹H-NMR spectrum for the following molecule…
A: we have to determine the splitting of the marked hydrogens in 1-HNMR spectrum
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- Explain why toluene did or did not react witj permanganate solutionsIn 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…Identify the organic functional groups and reaction type for the following reaction.The reactant is a(n)a. beta pyranoseb. beta furanosec. alpha pyranosed. alpha furanoseThe product is a(n)a. alpha furanoseb. alpha pyranosec. beta furanosed. beta pyranoseThe reaction type is:a. oxidation (benedict's)b. esterificationc. mutarotationd. reduction (hydrogenation)e. hemiacetal formation
- When cyclohexanone was reacted with an amine A. It the reaction formed an enamine, whichof the following is the most likely identity of amine A?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.dedcue the major organic product from the following reations. be ablw to draw hydration halogenation hydrohalogenation, halohydrin formation, oxymercuratiom demercuration qnd hydroboration oxidation.
- Provide the products, intermediates, and/or reagents forthe following reactions: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 waysMelamine, used as a fire retardant and a component of the writing surface of white boards, can be prepared from s-trichlorotriazine through a series of SNAr reactions with ammonia. The first substitution takes place rapidly at room temperature. The second substitution takes place near 100 °C, and the third substitution requires even higher temperature and pressure. Provide an explanation fatr this reactivity.
- The key step in a reported laboratory synthesis of sativene, a hydrocarbon isolated from the mold Helminthosporium sativum, involves the following base treatment of a keto tosylate. What kind of reaction is occurring? How would you complete the synthesis?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.How is compound A related to compounds B–E? Choose fromenantiomers, diastereomers, constitutional isomers, or identicalmolecules.