Decalin B-Pinene Camphene Trans-Stilbene 2. Write structures for all of the possible isomers of molecular formula...
a-pinene When a-pinene reacts with ї. ВНЗ; 2. H202, NaOH, H2O 4 possible cis,trans isomers can be formed, but one of these is formed in over 85% yield. Draw the structure of this preferred isomer. . Use the wedge/hash bond tools to indicate stereochemistry where it exists. - To aid you in your drawing, the structure of a-pinene is provided for you in the drawing palette.
Draw structures for all constitutional isomers with the molecular formula C2H6O.
Draw structures for all constitutional isomers with the molecular formula C2H4Cl2.
Draw structures for all constitutional isomers with the molecular formula C2H5Cl
1. Most of the class will be brominating trans-stilbene (part B) and the rest cis-stilbene (part A). For this assignment write a detailed procedure in your lab notebook for Part B. Upload a picture/scanned copy (5 pts). Tip: If you write the procedure down the left half of the page, you can leave space to record your measurements/observations down the right side of the page. If you end up using cis-stilbene in the experimental there will only be a few...
6. Draw and name all the alkene cis-trans isomers corresponding to the molecular formula C5H10. (Hint: there are only two.)
same compound, constitutional isomers (structural isomers), cis-trans isomers, not isomers (different molecular formula). Br a Br C C and Br Br
8) Give the relationship between the following pairs of structures. Possible relationships are: same compound, cis-trans isomers, constitutional (structural) isomers, not isomers (different molecular formula) and and CI Br CI and and СH, Br CHз and and CI CI and and
3. Draw all possible constitutional isomers of aldehydes and ketones with molecular formula C5H100 and name all isomers. 1. Identify a pair of skeletal isomers? 2. Identify a pair of positional isomers? 3. Identify a pair of functional isomers?
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