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- Which of these alkyl chlorides undergoes dehydrohalogenation in the presence of a strong base to give pent-2-ene (shown below) as the only alkene product? O l-chloro-2-methylbutane O 2-chloropentane O 3-chloropentane O 1-chloropentane O l-chloro-3-methylbutane9) Draw the conformer structure, Newman projection, before elimination and the elimination product of the following reaction: Br CH3ONA HWhich of the following is not a product of this elimination reaction? (C6H5- is a benzene ring) Cl CH3 | | CH3CH2CH2-CH-CH-C6H5 + CH3CH2OH → CH3 | CH3CH2CH=CH-CH-C6H5 CH2 || CH3CH2CH2CH2-C-C6H5 CH3 | CH3CH2CH2CH2-C=C6H5 C6H5 | CH3CH2CH2CH2-C=CH2 CH3 | CH3CH2CH2CH=C-C6H5
- What is the relationship between the products formed in the SN1 reaction below? Options: Structural isomers Enantiomers Diastereomers IdenticalExplain why methyl trifluoroacetate, CF3CO2CH3, is more reactive than methyl acetate, CH3CO2CH3, in nucleophilic acyl substitution reactions.Please help with part D attached:
- Above all, nomenclature-wise, the following compound is a(an) aldehyde alkene ketone aromatic conjugated aromatic ہےWhat is the purpose of CH3CH2OH in the reduction of a ketone? NaBH4 reduces while HCl protonates.. what about ethanol?9) Draw the "hexagon” line structure of the following (be sure to indicate stereochemistry). FOLOH ОН Br