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I need help with questions 4-9. PLEASE tell me how to do them I\'m so lost. Name

ID: 986808 • Letter: I

Question


I need help with questions 4-9. PLEASE tell me how to do them I'm so lost. Name caacesa CHM236 Quiz 2 Please answer the following questions. One point each, except as indicated 11) which of the following could be used to produce an aldehyde by oxidizing a primary alcohol? (A) Nitriu acid (B) Chromic acid (C) Potassium pe (E) None of these (D) Swern's reagent 2Why are tosyl esters very useful forms of alcohols? (A) The tosylate ion is a good leaving group (B) They give higher yields in substitution reactions (C) A wide variety of nucleophiles can be used to displace the tosyl group (D) Tosyl ester substitution reactions can be performed in acid O All of these 3Which of the following reagents is probably the best choice to prepare an alkyl chloride from an alcohol? (A) HCI (B) PC, (C) C,(D) sOCI, (D) Perchloric acid -2-methyl-2-butanol was heated with sulfuric acid, which of the following is the correct name for the alkene that is likely to be the major product? (A) 2-methyl-1-butene (B) 2-methyl-2-butene (C) 3-methyl-1-butene (D) 3-methyl-2-butene 5 An unknown alkene was reacted with KMnO. The product was treated with periodic acid. The only product of the reaction was acetone (2-propanone). What is the correct name of the unknown alkene? (A) 3-hexene (B) 2,3-dimethyl-2-butene (C) 2-methyl-2-pentene (D) 2-hexene What reagent could be used to form a phosphate ester from an alcohol? (A) Phosphorus trichloride (B) Phosphoric acid (C) Phosphorus acid (D) Elemental phosphorus when preparing an alkoxide from a tertiary alcohol, what reagent is likely to be the best choice? 7_When preparing an al 7 (A) K (B) Na (C) NaOH (D) A Grignard reagent What reagent system could be used to reduce an alcohol to an alkane? (A) H, with Pt (B) NaH (C) Tosyl chloride in pyridine followed by LiAIH (D) CuO and heat 9. Suggest a reasonable synthesis of ethyl isopropyl ether, beginning with alkanes, alkenes or alkyl halides. (2 points)

Explanation / Answer

Alcohols undergo dehydration which means water molecule is removed from the alcohol to form alkene.

2, methyl 2-butanol react with H2SO4 to give 2-methyl 2-butene