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19. The IUPAC name for (CH3)3COH is _____. a. 2-butanol b. 2-methyl-2-propanol c. 2-propyl-2-butanol d. 2-methyl-1-porpanol e. 2,2-dimethyl-2-ethanol

24. Which of the following alcohols produces no reaction when subjected to oxidation? a. methanol b. 2-methyl-2-propanol c. 2-propanol d. 3,4-dimethyl-1-pentanol e. 2-butanol

13. Which of the following alcohols is the active ingredient in most alcoholic beverages? a. Methyl alcohol b. Ethyl alcohol c. Isopropyl alcohol d. Butyl alcohol e. Cyclohexanol

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I would like to get help to write an abstract about this experiments. Please and thank you.

GOGGLES RE A. Structures of Alcohols and Phenol Draw primary B. Properties of Alcohols and Phenol Materials: 6 test tubes, pt paper, pH 1. Place 10 drops of ethanol, 2-propanol,ãbutyl alcohol (2-methyl-2-propanol).ã the condensed structural formula of each model in the display and for stirring rod, ethanol, 2-propanol, 2-methyl-2-propanol ( cyclohexanol, 20% phenol, and unknown, Caa ion: An ld contact with phenol secondary, or tertiary aleohol butyl alcohol), alan 20% tod to place a drop of each on a piece of phH paper. Clean the stirring rod between a the eolor of the pH paper with the color chart on the container to determine the pH observations. Save the test tubes and alcohols for part 2 phenol, and the unknown into six separate test tubes. Obtain some pH paper. Use a 2. A4 2 ml of water (40 drops)to each test tube, Shake and deternine the solubility a cloudy mixture or separate layer will form. Record your obse Solubility in water 2. Add 2 ml of with no separne each alcohol. If the compound is soluble in water, you will see a clear solution mixture layers. If it is insoluble, GNATED WASTE CONTAINERS DISPOSE OF ORGANIC COMPOUNDS IN DES C. Oxidation of Alcohols Materials: 6 test tubes, ethanol, 2 propanol, 2 ethyl-2-propanol (butyl alcohol), cyclohexanol, 20% l. Place 8 d ops of ethanol, 2-propanol, 2-methyl-2-propanol (ãbutyl alcohol), cyclohexanol, 20% phenol, unknown, 2% chromate solution phenol, and the unknown into six separate test tubes. Carefully add 2 drops of chromate solution to each. Stir carefully to allow the alcohol to react. Caution: Chromate solution contains concen trated HySO which is corrosive. Look for a color change in the chromate solution. If a test tube becomes hot, place it in a beaker of ice cold water. Record your observation of the color after 2 minutes. 2. Draw the condensed structural formula of each aloohol. 3. Classify each alcohol as primary (1"), secondary (29), or tertiary (3) If the orange color turned green within 2 min, oxidation of the alcohol has taken place. If the color remained orange, no reaction has occurred. If a reaction occurred, draw the condensed structural formulas of the product. When there is no change in color, no oxidation took place. In this case, write "no reaction" (NR) 4. DISPOSE OF ORGANIC COMPOUNDS IN DESIGNATED WASTE CONTAINERS! D. Iron(III) Chloride Test Materials: 6 test tubes, ethanol, 2 propanol, 2 methyl-2-propanol (1-butyl alcohol), cyclohexanol, 20% phenol, unknown, 1% FeCl3 solution Place 5 drops of the alcohols and unknown in separate test tubes. Add 5 drops of 1% Fecis solution each. Stir and record observations DISPOSE OF ORGANIC COMPOUNDS IN DESIGNATED WASTE CONTAINERS E. Identification of an Unknown Use the test results to identify your unknown as one of the five compounds used in this experimen Draw the condensed structural formula of the unknown. 90

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