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Preparation and Characterization of a 3 Alcohol

1H NMR spectrum and use the data to determine which alcohol you have produced. Be certain to consult with your instruotor before undertaking any procedures. [Pg.660]

1-Bromopropane 3-Pentanone 3- Methyl-3-heptanol 4- Methyl-4-heptanol 3-Ethyl-3-hexanol 2- Methyl-2-hexanol 3- Methyl-3-hexanol 2- Methyl-2-octanol 3- Methyl-3-octanol 4- Methyl-4-octanol 3-Ethyl-3-pentanol 2- Methyl-2-pentanol 3- Methyl-3-pentanol [Pg.660]

Dilute the combined aqueous layers and washes with water, neutralize the solution if necessary, and flush it down the drain with excess water. Place the ether distillate in the container for nonhalogenated organic solvents. Spread the calcium chloride from the drying tube and the sodium sulfate on a tray in the hood, and then place them in the container for nonhazardous solids after the volatiles have evaporated. [Pg.660]

Arrange the following compounds in order of increasing reactivity toward attack of a Grignard reagent at the carbonyl carbon atom methyl benzoate, benzoic acid, benzaldehyde, and benzophenone. Explain the basis for your decision, making use of mechanisms where needed. [Pg.660]

What is (are) the product(s) of reaction of each of the carbonyl-containing compounds in Exercise 1 with excess Grignard reagent, RMgBr  [Pg.660]


See other pages where Preparation and Characterization of a 3 Alcohol is mentioned: [Pg.659]    [Pg.943]   


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