Predict the major product(s) obtained the following compound undergoes hydrolysis in the presence of H30*: (A) O (B) OH (C) O но ÓH он (A) (B) (C)
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- Give the expected organic product when phenylacetic acid, PhCH2COOH, is treated with reagent Q.)LiAlH4 followed by H2OThe formula for the alarm pheromone for one species of ant is C7 H7 O. When treated with I2 and NaOH, this pheromone yields iodoform and n-hexanoic acid. What is the structure of the pheromone?Give the expected organic product when phenylacetic acid, PhCH2COOH, is treated with reagent Q.)NaOH, H2O
- Arrange the following molecules in increasing order of acidity. Base it only on their structural differences and explain how it is so. 1. HF, CH3CH2CH2OH, CH3CH2COOH 2. Ethyl amine, Ethanol, PropaneTreatment of 1-aminoadamantane, C10H17N, with methyl 2,4-dibromobutanoate in the presence of a nonnucleophilic base, R3N, involves two successive SN2 reactions and gives compound A. Propose a structural formula for compound A.As far back as the 16th century, South American Incas chewed the leaves of the coca bush, Erythroxylon coca, to combat fatigue. Chemical studies of Erythroxylon coca by Friedrich Wöhler in 1862 resulted in the discovery of cocaine, C17H21NO4, as the active component. Basic hydrolysis of cocaine leads to methanol, benzoic acid, and another compound called ecgonine, C9H15NO3. Oxidation of ecgonine with CrO3 yields a keto acid that readily loses CO2 on heating, giving tropinone. (a) What is a likely structure for the keto acid? (b) What is a likely structure for ecgonine, neglecting stereochemistry? (c) What is a likely structure for cocaine, neglecting stereochemistry?
- Give the expected organic product when phenylacetic acid, PhCH2COOH, is treated with reagent Q.)NaHCO3, H2O1- Arrange the following compounds in order of decreasing reactivity towards hydrolysis. 2- Arrange the following chemical species in order of decreasing basicity.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, Butane
- Rank the following compounds in terms of increasing acidity:I. C2H5OHII. C6H5OHIII. NaOC2H5IV. CH3COOHThe sex attractant of the common housefly is a hydrocarbon named muscalure, C23H46. On treatment of the muscalure with aqueous acidic KMnO4, two products are obtained, CH3(CH2)12CO2H and CH3(CH2)7CO2H. Propose a structure for the muscalure. Please provide a full explanation with steps when providing the structure as a response, thank you!Predict the products obtained from the reaction of triolein with the following reagents.(a) NaOH in water (b) H2 and a nickel catalyst (c) Br2 in CCl4(d) ozone, then dimethyl sulfide (e) warm KMnO4 in water (f) CH2I2>Zn(Cu)