

2. Draw the structures of the cis-trans isomers for each compound. Label them cis and trans. If no cis-trans isomers exist, write none. a. 2,3-dimethyl-2-pentene b. 1,1-dimethyl-2-ethylcyclopropane c. 1,2-dimethylcyclohexane d. 5-methyl-2-hexene e. 1,2,3-trimethylcyclopropane
Label the compound as cis or trans.
Be sure to answer all parts.
For each compound shown below, draw representations for the
cis and trans isomers using a hexagon for the six-membered ring,
and wedges and dashes for substituents.
[1] cis:
draw structure ...
trans:
draw structure ...
[2] cis:
draw structure ...
trans:
draw structure ...
1 attempt left Check my work Select the single best answer. Label the compound as cis or trans. ints eBook нот HO cis...
1. Name the molecules shown below Br Br 2. Draw and label both the cis and trans forms of 1-isopropyl-2-methylcyclobutane.
draw the cis and trans isomers of 2-pntane and label them. b. draw trans -4,4 dimethyl-2-pentane c. draw cis -2- hexane
For the molecules whose condensed structural formula is given below, decide if cis-trans isomers are possible. If they are, enter the name of the cis isomer in the first box and the name of the trans isomer in the second box. a) CH3CH=CHCH3 name of cis isomer or molecule: name of trans isomer or none: b) (CH3)2C=CCl2 name of cis isomer or molecule: name of trans isomer or none:
Name or draw the following molecules (use cis/trans
naming system)
1. Name or draw the following molecules (use cis/trans naming system): CI CI CH3 CH2CH3 a. b. c. 4-ethyl-6-(1,2-dimethylpropyl)decane 2. Draw all of the resonance structures for the following compounds. CH2
Choose all of the molecules that can have both
cis and trans configurations.
I understand the cyclohexane does not fit the requirements, and
neither does a molecule with a triple bond. But does the molecule
with a ketone? I feel like A-C fit the requirements for having both
cis and trans configurations.
Choose one or more: ОА. H₂C сна B. C O C. OD I E. Học ==CH, OF.
7. Draw and label both cis and trans isomers of 1-ethyl-4-methylcyclohexane. (10 pt) a. For each isomer, draw the two possible chairs and indicate which of the two will be preferred and by how much (a lot or little). (5 pt) b. Which of the four is considered the most stable (label as "best") and which is least stable ("worst")? (3 pt) c. Clearly label 1,3-diaxial interactions, if present, in any of the conformations? (2 pt) Cis Trans
5. Name the following alkene molecules. Be sure to include cis/trans designations whenever necessary! CH3 CH3 Br CI
Molecules that differ in configuration CANNOT be: a. stereoisomers b. cis-trans isomers c. chiral centers that are mirror images of each other d. enantiomers e. chiral centers that can be interchanged by rotation of a single bond