Please draw: (Z)-1-chloro-3-ethyl-4-fluoro-3-octene
1) Draw structures for compounds named below. A) (Z)-1-bromo-2-chloro-1-heptene B) 4-chloro-4-fluoro-2-octyne
4. Draw the line-angle structure for each of the following a) (2E,4Z)-4-ethyl-5-isopropyl-3,6-dimethylocta-2,4-diene b) (2Z,4Z,6E)-3-bromo-5-chloro-4-ethyl-7-fluoro-9-methyldeca-2,4,6-triene c) (5S,8S)-3-sec-butyl-5-ethyl-1,8-dimethylcycloocta-1,3,6-triene d) 2-ethyl-3,5,5-trimethylcyclopenta-1,3-diene
Please provide a structure for each of the following names. 1-Bromo-3-methylcyclohexene 3-Ethyl-2-pentene cis-3-Octene (Z)-3-Methyl-2-hexene Vinylcycloheptane (Z)-1,3,5-Tribromo-2-pentene 1,2-Diethyl-cyclopentene Vinybromide 2,3-Dimethyl-2-butene 3,7,7-Trimethyl-4-octene 4-lsopropyl-1-nonene (E)-3-Methyl-2-heptene
1) Draw structures for compounds named below. A) (2)-1-bromo-2-chloro-1-heptene B) 4-chloro-4-fluoro-2-octyne 2) Give IUPAC name for the following structure. 3) For each reaction below, indicate which starting material is the Nucleophile and which is the Electrophile. Show arrows to demonstrate how the transformation occurs. →^_^tts a Porto ~ onde gi 4) Draw a mechanism for the conversion of the shown starting material to the corresponding product. 5) In the transformation below, a starting material is treated with HCl to form...
Draw both cis and trans isomers for 3-ethyl-2,5-dimethyl-4-octene (hope i spelled that molecule correctly).
0 2. Draw the structure for a) (2)-1-chloro-2-ethyl-1,3-butadiene b) glycerol c) (Z)-2-ethyl-2-buten-1-ol
Draw structures for the following compounds. a. 2-chloro-1,3-cyclopentadiene b. 2-bromo-5-nitroaniline c. 2-chloro-5-fluoro-3-octyne
3. Write the structure of following organic compounds (15 points) 3-Chloro-5,7-dimethyl-4-cyclopropyl-2-octene 2-amino-3-methyl-2-nitro-butanal 2-Bromo-4-nitro-3-hexanol Aminomethanamide 2-Chloro-3-methyl-1-cyclopentanone 2-bromo-3-methyl-2-pentene 1-ethyl-3-methyl-2-propylcyclopentane 2-Keto-1,3-propandioic acid
Draw the following molecules: 1. (Z)-3-heptene 2. (R)-3-fluorocycloheptene 3. (R)-2-ethyl-2-hexanol 4. trans-1,2-dimethylcyclohexane 5. 1,1-dipentylcyclopropane 6. (R)-1-chloro-2-methylpropane 7. (2R,3S)-2,3-dibromobutane
8. (a) Draw the structure of (4R,5R)-4-ethyl-5-fluoro-2-methyl heptane. Use solid and dashed wedges to show the proper configurations of the chiral centers. (0.4 pts) (b) Now draw a Newman projection for the most stable conformation of the C(4)-C(5) bond. (0.4 pts) H (c) Draw a diastereomer of (4R,5R)-4-ethyl-5-fluoro-2-methyl heptane (0.2 pts)