Can someone help me draw these?
1. (1S)-5-(p-methylphenyl)cyclopent-2-enol
2. (Z,2R,7S)-2-hydroxy-7-methyl-3,8-dioxooct-4-enoic acid
Note for assigning R/S
If last (4) priority is below the plane I.e., on dash the clockwise rotation of priority 1 2 and 3 gives R and counterclockwise rotation gives S
If last priority is above the plane I.e., on wedge then clockwise rotation of priority 1 2 and 3 gives S and counterclockwise rotation gives R configuration. That means what the configuration of a chiral carbon will be depends on where the last priority is located
P.S. priority of the atoms of chiral carbon is assigned according to CIP rule.
You don't have to mention the numbering of parent carbon chain. I mentioned it just to make you understand. Please like the answer if it helped. Thank you. :)
Can someone help me draw these? 1. (1S)-5-(p-methylphenyl)cyclopent-2-enol 2. (Z,2R,7S)-2-hydroxy-7-methyl-3,8-dioxooct-4-enoic acid
Draw the following compound: (Z,2R,7S)-2-hydroxy-7-methyl-3,8-dioxooct-4-enoic acid.
Draw the structures for the following compounds. a) (3Z,5S)-4-bromo-5-chloro-2-methylhexa-1,3-diene b) (5S,7S)-5-(bromomethyl)-7-chloro-oct-2-yne c) (1S,5S,6S)-6-bromo-5-[(1R)-1-chloroethyl]cyclohex-3-enol d) 2-bromo-4-[(1R)-1-hydroxyethyl]benzoic acid e) (3S,4S,5S)-5-amino-3-hydroxy-4-methylhexanal f) (Z,2R,4R)-6-bromo-4-chloro-N-ethyl-N-methylhept-5-en-2-amine g) [(1S)-1-chloroethyl] (Z,3R)-5-chloro-3-methoxyhex-4-enoate h) (Z,3R)-3-bromo-4-chloro-7-methyloct-4-enoic acid i) (3S)-6-bromo-N-ethyl-N,3-dimethylhex-4-ynamide j) (Z,3R,4S)-6-bromo-3-[(1S)-1-chloroethyl]-4-hydroxyhept-5-en-2-one
Draw (Z)-5-[cyclopent-1-enyl]hex-4-enoic acid. Remember to add all bonds to stereocenters (including bonds to hydrogens).
Can someone please help me draw the Fischer projection for (2R,4S) methyl-4-amino-4-chloro-2-methoxypentanoate? I understand the nomenclature and process on how to draw a Fischer projection, but I am stuck on where to draw the CH2 between both chiral centers. Thank you!
can someone help me figure out how to draw these
please
3-methylbutan 4-methyl-2-pentanone propanoic acid ethylpropanoate dimethylethanamide
1. Draw the following molecules, based on their IUPAC name: a) 2-hydroxy-5, 5-dimethylheptanedioic acid; b) 3-hydroxy-7-methylnonanedioic acid 2. Give the IUPAC name for the following compounds: A) HO OH 3. Circle the name that is correct for each molecule, based on IUPAC rules. V a) 4-methylheptanoate 4-methylbutanoate b) pentyl 4-metylhexanoate c) 3-methylbutyl 4-methylhexanoate d) isobutyl 4-methylhexanoate
can someone help me draw out the mechanism for p-anisidine and 1-bromo-2,4-dinitrobenzene with ethanol?
4) Draw the following compounds a. (2S,5R)-5-chloro-2-ethylhexanoic acid b. (1R,2R,4R)-4-ethylcyclohexane-1,2-diol c. (2S,3R)-3-amino-2-phenylbutanal d. (1S,2S,3R)-2-fluoro-3-propylcyclobutanol e. (2E, 7Z)-5-bromo-2,7-nonadiene
Draw the following structures: 1. N-methyl-1-propanamine 2. N,N-dimethylmethanamine 3. 4,4-dibromohexano ic acid 4. 2-methylpentanoic acid 5. 2-chloroethanoic acid 6. Methyl methanoate 7. Ethyl benzoate 8. Pentyl butanoate 9. Aniline 10. Methanoic acid 11. N-ethyl-3-hexanamine
can
someone help me with this question please
3. Draw the structu res of the four compounds - acetic acid, decane, 2-octanone, and 1- butanol. Arrange them in order of increasing R of the thin layer chromatography by placing the appropriate number under the structure. Let 1= smallest R.