2. Draw the bond-line formula for each of the following: a. Pentanoic acid: b. 2-bromo-3-methylhexanoic acid: c. 4-...
i)Draw bond-line structures for each of the following: [4 marks] a) 2-butyloxiraneo ZWn c) 2-methyl-3-hekyn-2-ol b) Ethylhexanoate d)2-chloro benzoic acid
Draw the Bond-Line structures for the following compounds. a) 1-Bromo-6-(2,2,3-trimethylbutyl) undecane b) (CH3)2CHCHC(CH3)2 c) 2,5-dicyclobutyl-4-ethylheptane d) 1-tert-butyl-3-fluorocyclohexane
(40 pts.) Give the structure of the following in condensed or bond line formula: 2-bromo-7-phenyl-4-nonyne
Draw the condensed structural formula, or line-angle formula, if cyclic, for each of the following. Part A 1-methylcydlopentene Part B 1-bromo-3-hexyne Part C 3,4-dimethyl-1-pentene
Draw all possible stereoisomers for each of the following.(a). 2- chloro-3-hexanol. (b). 2-bromo-4- chlorohexane . (c) 2,3,-diachloro pentane. (d). 1,3-diabromopentane.(2) .Draw the stereoisomers of 2-methylcyclohexane.
Draw the condensed structural formula far each of the following compounds. a. 2-nonene b. 2, 3, 4-trimethylpentane c. trans-1-choro-3-ethylcycloheptane d. 4-isopropyloctane e. 1-bromo-2, 2-dimethylbutane f. cis-1-bromo-3-chlorocyclohexane g. g. A compound is incorrectly named 2-ethyl-2, 4-dimethylhexane. Draw the molecule and label with the correct IUPAC name.
a propyl ethanoate (full structural) b 3-ethyl-2-methylhexanoic acid (line) C 2-bromocyclopentene (condensed structural) d 2-methyl-3-phenylpentane your choice) Butane-1,2,3-triol (your choice) [insert a photo of your work here] a b е red, greenF. grey C, white d H HH e
help please!
Draw the Fischer projection for (2S, 4R)-2-bromo-4-ethyl-4-methyloctane 13. (6) Draw the line-angle formula for: (4R, 5S), 2,4,5-trimethylheptane
1) 2-amino-3-hydroxybutanoic acid
2) 2,3-dinitrobutane
A. Draw the skeletal structure (line-bond) for the following compounds. B. Convert the structures to the Most Stable and the Least Stable Newmann projections around (looking down) C2-C3 bond. (The numbering is based on the nomenclature locator numbers) C. On your skeletal structures, label the stereogenic centers (chiral carbons) if there are any. D. Draw all the possible stereoisomers for the compounds. Indicate which are enantiomer pairs. which are diastereomers to each other, and if...
Can someone please check this?
b. Draw 3-bromo-2-iodopentane in the box provided in skeletal structure. Then draw the Newman projection Max would see if he looked down the C2-Cs bond of 3-bromo- 2-iodopentane (HINT: there are many possible stereoisomers you could choose to draw. Pick one and be consistent.) Highest energy conformation i. CH Br il. Lowest energ conformation CH Сснз) 01Hy c. Draw the line structure of the following Newman projection that Max drew for you iPrt e d...