Draw the skeleton structure of 3-methyl-2-hexanone or 3-methylhexan-2-one.
Draw the structure of the organic product(s) of the reaction between (S)-3-methylhexan-2-one and phenylmagnesium bromide, followed by acidification. Use the wedge/hash bond tools to indicate stereochemistry where it exists. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the + sign from the drop-down menu.
Lumili alle for the following compound? - (CH)CHCH.COCH,CH, a. 2-methyl-4-hexanone c. 2-methyl-3-hexanone b. 5-methyl-3-hexanone d. ethyl isopropyl ketonel. 25-Identify the directing effect of the ring substituent in the following reaction: BO, HBO. (a) o.p., activating (b) m-, deactivating (c) o.p., deactivating (d) None of these 26--Ketones are easily reduced to CH3-C-CH3 a-Secondary alcohol b- Primary alcohol c- to acetaldehyde d- to carboxylic acid 27-. What is the structure of the azo group? a-N- b-N-N- C-NEN- d-NEN- 28-What class of organic...
Draw the structure of the organic product(s) of the reaction between (R)-3-methylhexan-2-one and phenylmagnesium bromide, followed by acidification • Use the wedge hash bond tools to indicate stereochemistry where it exists. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right comer, • Separate multiple products using the + sign from the drop-down menu. ( Oo * ChemDoodle Submit Answer Try Another Version 9 item attempts remaining
Question 3 1 pts What is the IUPAC name for the following compound? O (3S,4R)-3-bromo-4-methylhexan-2-one O (3S,4S)-3-bromo-4-methylhexan-2-one (3R,45)-3-bromo-4-methylhexan-2-one O (3S,4R)-3-bromo-4-methylhexan-2-one 3-bromo-4-methylhexan-2-one 0 4-methyl-3-bromohexan-2-one
11) (24 pts total) (A) Consider the following compounds: 4-heptanone 3-hexanone 2-hexanone cyclohexanone methyl acetate (a) (4 pts) Circle the compound that could be subjected to a haloform reaction (b) (12 pts) Provide the structure of the product obtained when the compound chosen in (a) undergoes the iodoform reaction; include the correct steochiometry for all the reagents used in the reaction. (B) (8 pts) Provide the strctures of compounds A and B obtained in the reaction sshown below.
Question 3 (2 points) Choose the best name for the compound drawn. 6-methyl-3-propyl-2-heptanal 2-methyl-5-octanone 6-methyl-3-propyl-2-heptanone 3-isopentyl-2-hexanone
Draw (3R, 4S)-4-methylhexan-3-ol
Draw the structure of 3‑methyl‑1‑butyne.
Draw the structure of 3-methyl-1-butyne. Rings Select Draw More Erase privacy policy terms of use contact us help about us careers
An ester and 2 equivalents of a Grignard reagent reacted to form 4-propylheptan-4-ol and 3-methylhexan-3-ol after acid workup. (a) Draw the skeletal structure of the ester. (b) Draw the skeletal structure of the Grignard reagent.
Be sure to answer all parts. Draw the structure of 4-methyl-2-heptanol. Then draw and name the product that you would expect to produce by its oxidation. Part 1: Structure of 4-methyl-2-heptanol: view structure Part 2: Structure of oxidation product: no structure shown Part 3: Name of product: 4-Methy-3-heptanal 4-Methylheptanone 4-Methyl-3-heptanone 4-Methyl-2-heptanone