Answer the following Questions 1. Which of the following would you predict to be more soluble...
which of the following is the structure of 2-ethylbenzamide 3. (20 points) The following alcohol undergo chromic acid test. Complete the blank for each alcohol Color after reaction is test positive or negative? Class of Alcohol CH₂ - CHCH, CH, CH, ан,— —днан, Color after reaction is test positive or negative? Class of Alcohol Color after reaction is test positive or negative? Class of Alcohol at CH2OH & CH₂ CH3 6th c Color after reaction is test positive or negative?...
3. Which of the following alcohols is least soluble in water ? a. 1-pentanol c. 1-hexanol b. 1-octanol d. 2-propanol
1. Draw the structures of the following alcohols: ethanol 2-propanol cyclohexanol 2-methyl-2-propanol Classify each of the alcohols in question 1 as primary, secondary, or tertiary. ethanol 2-methyl-2-propanol 2. 2-propanol cyclohexanol 3. Which alcohol would you expect to be more soluble in water, 1-butanol or 2-methyl-2- propanol? Why? (Hint: draw both alcohols examine their structures).
Which of the following alcohols would have the lowest solubility in water? A) 1-hexanol B) isopropyl alcohol (2-propanol) C) 1-butanol D) ethanol
i believe its 3,3-dimethyt-2-butanol 0r 4 methylbeNzyl alcohol based on the data provided. if not which alcohol would it be for the unknown compunds. #3 Unknown Al Data unknown Melting point of solid ("C) (leave blank if liquid at RT): 57 degrees Celsius Boiling point of liquid (C) (leave blank if solid at RT) 0-H Stretch alcohol The results from sodium fusion and follow up ion tests (578) Predicted color Nitrogen test absent Nitrogen red brown precipitate Sulfur test black...
Part 2 Multiple Choice. Select the best answer for each of the questions below: 1. Which of these molecules is not an electrophile? a) CH4 b) CH3+ c) H* d) BF3 2. Which of these molecules is not a nucleophile ? a) NH3 b) OH c) CN d) H* 3. Water behaves as: a) a nucleophile b) an electrophile c) both d) neither 4. The SN2 reaction has how many steps? a) 1 b) 2 c) 3 d) 4 5....
For O. Chem lab titled: "Perfumes: The Synthesis of Nerolin". Please answer questions 16 (a-c) and 17. Nerolin chemically is called either 2-ethoxynaphthalene or ethy! S-naphthy! ether and can be prepared by the following Williamson synthesis of ethers. OH O-CH.CH - 1-CH.CH KOH alcohol +H.O+KI Waphthal Ethyl iodide Nerolin The potassium hydroxide, acting as a base, removes the slightly acidic proton from 6-naphthol and converts it into the nucleophile potassium B-naphthoxide, which attacks ethyl iodide and displaces the iodide ion....
1. Given the following structures that react by Sn1, which would react fastest and which would react slowest. Give reasoning. 5-bromo-1,3-pentadiene, bromocyclopentane, (R)-2-bromo-2-methylhexane. 2.If bromocyclohexane reacts faster than chlorocyclohexane in an Sn2 reaction, what could be the reason? 3.You wish to substitute the bromine in the following molecules with a nucleophile. Explain whether the given molecule would react by Sn1 or Sn2 mechanism and explain why. 1-methyl-1-bromo-cyclohexane, 1-bromopropane, 2-bromohexane. 4. Why does benzyl bromide react under both Sn1 and Sn2...
Questions for the lab: 1. Give a structure for each of the following formulas that show only one (1) peak in the proton NMR. a. CH&0 b. C110 2. How would you distinguish between each of the following compounds using H-NMR? a. O CH3 and Cl 12-C-OH methyl benzoate phenylacetic acid b. CH2-C-OH and H;C phenylacetic acid CH3 4-methylbenzoic acid ta c. CH3-C-CH3 and CH3-CH2-CH-??? 2-butanol ?? t-butyl alcohol and H3C CH3 1,4-dimethylbenzene 1,2-dimethylbenzene 3. Identify a compound, C,H2O, that...
I need help answering the following questions 1) A compound is insoluble in water, soluble in conc. H2SO4. It shows positive for the 2,4-DNPH test and negative for Chromic Acid test. What do you think the compound is? (3 pts) a) Isopropyl alcohol b) Butyraldehyde c) 3-pentanone d) butan-1-ol 2) Which compound would give a negative result for Iodoform Test? (3 pts) a) t-butyl alcohol b) Acetophenone c) 2-butanol d) Acetaldehyde 3) Which of the following routes can be used...