Solvolysis of 2-bromo-2,3-dimethylheptane in 1-propanol gave three products. Select the three products generated from this reaction. 2,3-dimethyl-2-heptanol (or 2,3-dimethylheptan-2-ol) 2,3-dimethyl-3-heptanol (or 2,3-dimethylheptan-3-ol) 2,3-dimethyl-2-heptene (or 2,3-dimethylhept-2-ene) ☐ 1,1,2-trimethylhexyl propyl ether (or 2,3-dimethyl-2-propoxyheptane) 2,3-dimethyl-3-heptene (or 2,3-dimethylhept-3-ene) 2,3-dimethyl-1-heptene (or 2,3-dimethylhept-1-ene) G

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When 2-bromo-2-methylbutane is treated with a base, a mixture of 2-methyl-2-butene and 2-methyl-1- butene is produced. When potassium hydroxide is the base, 2-methyl-1-butene accounts for 45% of the product mixture. However, when potassium tert-butoxide is the base, 2-methyl-1-butene accounts for 70% of the product mixture. What percent of 2-methyl-1-butene would be in the mixture if potassium propoxide were the base? base Br A. Less than 45% B. C. 45% Between 45% and 70% D. More than 70%

Complete the following reaction sequence with the missing major organic products. CH, NaOH CH,CH,CH,CHCH,CHCH,CEN H20 NaOH H,0 CH,CH,

Rank this compounds in order of increasing solubility (1-lowest and 4-highest) 3-hexanone > < butanone < propanone Question 9 Rank this compounds in order of increasing solubility (1-lowest and 4-highest) butanal 2-pentanone propanal ethanal methanal

Acid-catalyzed dehydration of 3,3-dimethyl-2-butanol gives three alkenes: 2,3-dimethyl-2-butene, 3,3-dimethyl-1-butene, and 2,3-dimethyl-1- butene. Draw the structure of the carbocation intermediate leading to the formation of 2,3-dimethyl-2-butene. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. If more than one structure fits the description, draw them all. Separate structures with + signs from the drop-down menu. C P opy aste ChemDoodle >

Acid-catalyzed dehydration of 3,3-dimethyl-2-butanol gives three alkenes: 2,3-dimethyl-2-butene, 3,3-dimethyl- 1-butene, and 2,3-dimethyl-1-butene. Draw the structure of the carbocation intermediate leading to the formation of 2,3-dimethyl-2-butene. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • If more than one structure fits the description, draw them all. • Separate structures with + signs from the drop-down menu. / H₂C CH₂ CH3 CH3 ChemDoodleⓇ On []

1-Phenyl-1-pentanol may be prepared using 1 - bromobutane along with simple organic/inorganic reagents. Draw the products and reactants that are used to synthesize 1-phenyl-1-pentanol. Be sure to answer all parts. Part 1 out of 2 → Mg diethyl ether 3 attempts left 1-Phenyl-1-pentanol may be prepared using 1-bromobutane along with simple organic/inorganic reagents. Draw the products and reactants that are used to synthesize 1-phenyl-1-pentanol. Be sure to answer all parts. Part 1 out of 2 Br Mg diethyl ether 3 attempts left Check my work draw structure ... Next part

Complete the following reactions with the appropriate reagents or products. 1 mol HBr H₂C 2 H₂ Pd 2 mol HCI ECH ? H₂C BH₂ H₂O₂, H₂O -CH ₂

Which of the following alcohols will be oxidized by potassium permanganate to form an aldehyde and then a carboxylic acid? OH H3C-CH₂-CH-CH₂-CH3 H3C-CH₂-CH₂-CH₂-CH₂-CH₂-OH OH CH3 H₂C-CH-CH-CH₂ CH3 OH H3C-CH-CH₂-CH₂-CH-CH3