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does 3-chloro-2,6-dimethyloctane have any chiral centers? if so where are they?
i need help with the chiral centers? how many chiral centers
does this compund have
3. How many stereoisomers are possible for this compound? (a) 4 (c) 8 (b) 16 (d) 32
penauere more reactive Wire any chiral centers does endo-norbornene-cis-5,6-dicarboxylic acid possess? Is the molecule itself chiral? (continued) 51
5. Do the following compounds have any chirality centers? Which one is chiral? If has chirality, how m stereoisomer does it have? (a) Cis- 1,2-dimethylcyclobutane (b) Penicilin G CH3 OH 2
(d) Do the following compounds have any chirality centers? Which one is chiral? If has chirality, how many stereoisomer does it have? (a) Cis- 1,2-dimethylcyclobutane (b) Morphine N- CHI OH Y CU HU
the following compound: a. Circle all chiral centers, if any b. is the overall compound chiral or achiral? 7. Based on your previous answer, can the compound in #3 rotate plane polarized light? yes or no)
Where are the chiral centers located?
NH HO Na
3.14 Which compounds contain chiral centers? (a) 2-Chloropentane (b) 3-Chloropentane (c) 3-Chloro-1-pentene (d) 1,2-Dichloropropane 3.18 Mark each chiral center in the following molecules with an asterisk. How many stereo isomers are possible for each molecule? CH COOH CH 0 (a) CH CCH=CH, (b) HCOH (c) CH,CHCHCOOH (d) CH,CCH.CH OH CH NH CH,OH OH CH,COOH (e) HCOH () CHCH.CHCHECH, (g) HOCCOOH CH,OH CH,COOH
Chiral or not? Mark the stereogenic centers if any are
present.
OH OCH
consider the molecule with two chiral centers. draw all remaining
possible stereoisomers using solid and dashed wedges
label each chiral center as R or S
5. Consider the molecule 1-chloro-3-tertbutylcyclohexane with two chiral centers: a. Using COMPOUND A (below) as a starting molecule, draw all remaining possible stereoisomers using solid and dashed wedges (no chairs). Compound B Compound A Compound C Compound D 6. On BOTH COMPOUND A and COMPOUND D (above), clearly label each chiral center as either R...
Determine the products of the following reactions. Identify any chiral centers in the products that will lead to a racemic mixture of products. There is no need to show your work.___