Ester Carboxylic Acid Alcohol Ester Formed Reaction 1 Ethanoic acid Pentan-1-ol Methanoic acid Propan-1-ol 3 Salicylic acid Methanol 4 Methanoic acid Phenol 2-methyl propan-1-ol (isobutanol) Ethanoic acid 6. Propanoic acid Octan-1-ol
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What is the IUPAC naming of this table?
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- i) 3-methyloctane-2,3-diol 11) 3-chloro-4-ethoxy-2-methylcyclopentanamine iii) N, N, 3,3-tetramethylbutan-2-amine iv) 1-ethoxy-2,5-difluorohexan-3-ol 6) 5-isopropoxy-3-isopropyl-6-propoxy-4-propylcyclohexane -1, 2-diol draw of the following names in skeletal formsSHOW COMPLETE SOLUTIONS Q3. Which isolate has A260/280 ratio of above 2.0?Describe the trends in the acidityand physical properties of carboxylicacids, and explain how their acidityvaries with their substituents.
- The Ka1 of ascorbic acid is 7.94 x 10-5. Would you expect ascorbic acid dissolved in blood plasma (pH 7.35–7.45) to exist primarily as ascorbic acid or as ascorbate anion? Explain.help me explain and draw the Synthesis: A Limonene Isomerpropenoic acid + methanol + acid catalysis = limonene isomer intermediate #1limonene isomer#1 + 2-methylbuta-1,3-diene + pressure = limonene isomer intermediate #2limonene isomer intermediate #2 + excess methyl magnesium chloride + mild hydronium workup = limonene isomer intermediate #3limonene isomer intermediate #3 + acid catalysis + heat= a limonene isomerGive the structure corresponding to each name.a. cyclohexyl propanoateb. cyclohexanecarboxamidec. 4-methylheptanenitriled. vinyl acetatee. benzoic propanoic anhydridef. 3-methylhexanoyl chlorideg. octyl butanoateh. N,N-dibenzylformamide
- Arrange the following molecules in increasing order of acidity. Base it only on their structural differences and explain how it is so. 1. Butanoic acid, Propionic acid, Propylamine, ButaneDraw the following compounds 1. butylethylmethylamine2. 4-iodohexanoic acid3. N-methylheptanamide 4. pentylpropanoate 5. propyne6. ethylene7. 1-heptanol 8. butyloctylether9. trans-3-nonene10. 1-choro-2-bromo-3-fluoro-4-iodo-hexane 11. butanal 12. 1-chloro-2-pentanonebased on this video: on Hinsberg Test Tests for Amines - MeitY OLabs (8.5min) https://www.youtube.com/watch?v=j5jgMUWri8U Write the reaction (two-step, in skeletal) of each test amine when tested in the Hinsberg Test.
- Electrostatic potential maps of anisole and thioanisole are shown. Which do you think is the stronger acid, p-methoxybenzoic acid or p-(methylthio)benzoic acid? Explain.Identify the organic functional groups and reaction type for the following reaction.Please include everything including the letter and the answers.The reactant is a(n)a. amideb. aldehydec. alcohold. carboxylic acide. esterf. ketoneThe product is a(n)a. carboxlyate ionb. ammonium ionc. alcohold. carboxylic acide. ketonef. aldehydeThe reaction type isa. hydrationb. esterificationc. hydrolysis (in acid)d. hydrolysis (in base)e. amide synthesisf. amide synthesisg. dehydrationh. acid basesynthesize each from benzene and sketch the following: H-NMR; C-NMR; MS, and IR for the compounds: 1. ortho form of aminophenol 2. meta form of salicylic acid