Draw the enantiomer of the molecule hown below. Use a dash or wedge bond indicate stereochemistry of substituents asymmetric centers, where applicable. ОН OCH3
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- By considering the stereochemical requirements for E2-elimination, and using an appropriate illustration need help indicating whether the more stable conformer (conformer B) of trans-1 can undergo E2 elimination. Thank you :)Two conformations of cis-l, 3-dimethylcyclobutane are shown. What is the difference between them, and which do you think is likely to be more stable?Rank the following groups in order of decreasing priority. −CH=CH2, −CH3, −C≡CH, −H
- Draw the skeletal (line-bond) structure for (5S), (3Z)-5-chlorohex-3-en-2-one. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable. Show proof for (5S) and (3Z).Draw the enantiomer of the molecule shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable.Draw the product formed when diene M undergoes disrotatorycyclization. Indicate the stereochemistry at new sp3 hybridized carbons.Will the reaction occur under thermal or photochemical conditions
- Based on the more stable conformation (conformation A), need help providing two mechanisms for the E2 elimination of the protonated version of cis-1 using a general base (B:) to give alkenes 2 and 3. Clearly show which hydrogens meet the stereochemical requirements for E2-elimination Using Zaitsev’s rule, indicate which is favoured. Pictured is also a reaction mechanism to show what the alkenes 2 and 3 are. Thank you :)SEE PHOTO: Draw the enantiomer of the molecule shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicablePredict the products of the reactions below. Show stereochemistry, using wedges and dashes, in the products and draw both enantiomers
- Draw all of the other stereoisomers of the structure shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable.Rings + Unsaturation --- Hydrogenation If compound A C51H81BrN5O3P3 is hydrogenated to give compound B C51H101BrN5O3P3. How many rings does compound A have? Assume that P has a valency of 5. Would the answer be 4 rings? Formula -> unsat + rings = 1+C +N/2 - H/2 - X/2label the stereocenters r,s,e,z and specify if any are meso. whats are the products to each orher? draw the chair conformationd and explain which one is the most stable for both products. are ha and hb homo/enantio/diasterio/hetero topic? also hc and hd.