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- Is the following alkene E,Z, or neither? a. E b. Z c. neither d. It is one or the other, but which is impossible to determine from the information givenName the alkene below.Use only E/Z designators to indicate stereochemistry.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
- Draw the product formed when diene M undergoes disrotatory cyclization. Indicate the stereochemistry at new sp3 hybridized carbons. Will the reaction occur under thermal or photochemical conditions?Alcohols can be converted to alkyl chlorides using SOCl2 with complete inversion of stereochemistry. Using curved arrows draw the stepwise mechanism for chlorination of an alcohol. Be sure to include lone pairs necessary to the mechanism steps and any non-zero formal charges.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 :)
- OChem HELP... Draw the conformational structures (chair or boat conformations) for the MAJOR product formed when 1-tert-butylcyclohexene reacts with each of the following reagents. Also, indicate if the product obtained is racemic form. a) Br2, CCl4 b) Br2, H2O c) OsO4, then aqueous NaHSO3 d) ICl e) mCPBA, then H3O+, H20 f) O3, then Me2S (conformational structure not required) g) BH3:THF, then H2O2, HO- h) D2, Pt i) Hg(OAc)2 in THF-H2O, then NaBH4, HO- j) BD3 :THF, then CH3CO2TTwo 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?Is it option (b)1-bromo-6-chlorocyclohexene?
- Stereochemistry: Assign each of the following alkenes as E or Z or unassignable. Also assign each of the following alkenes as cis or trans or not applicable.Compounds A and B are isomers having molecular formula C5H12. Heating A with Cl2 gives a single product of monohalogenation, whereas heating B under the same conditions forms three constitutional isomers. What are thestructures of A and B?b. In a strongly basic solution, the starting material again converts into a molecule with the molecular formula C6H12OC6H12O. but with a completely different structure.