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- On the lines drawn below, provide the systematic (IUPAC) names for the following structures. Be sure to include stereochemistry (R/S, cis-trans, or E/Z) when appropriate. Show some work for full.Chlorobenzene give reaction with kmno4 or not??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 :)
- give the organic product/s of the following reactions (include stereochemistry where appropriate) , please help with all partsSuggest a synthesis for the molecule below starting from benzene, alcohols of four carbons or fewer and any inorganic reagents for questions D-H please provide the full names for the compounds belowUnknown compound D,whose formula is C28H44O, is an alcohol that produces a compound whose formula is C28H50O upon catalytic hydrogenation with excess H2 over Pt.Indicate how many rings and pi bonds compound D contains based on the data given.
- Propose structure(s) for the compound and give the physical properties, chemical properties, and hazards for the compounds you propose (do not use Wikipedia). Describe in detail how you arrived at this structure (functional groups from IR spectra, degree of unsaturation, etc.).Birch reduction of 2-methoxynaphthalene gave a mixture of two isomeric compounds, each having the molecular formula C11H14O. Suggest reasonable structures for these compounds.Provide the E2 mechanism for β-elimination reactionemploying 2-chloro-2-methylbutane to prepare 2-methyl-2-butene and 2-methyl-1-butene reaction. Use the actual structures of thereactants and products. Explain which of the alkenes is the major product ofthis reaction ?
- 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).please provide the machanisms of 1a, 1e, 1fOn the lines drawn below, provide the systematic (IUPAC) names for the following structures. Be sure to include stereochemistry (R/S, cis-trans, or E/Z) when appropriate. Show work for full credit.