Don't provide handwritten solution ... Draw the correct structure for each of the following compounds. trans 3-cyclobutyl 2,6-dimethyl 4-heptenal
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- What is the structure of (s) 1-chloro-2-propanol with wedge and dash bondsProvide the correct IUPAC name for the skeletal (line-bond) structure shown here.a) This part of question refers to the molecule drawn below. CH3 CH,CH,CH3 CHFCH CH,CH3 i) Work out the absolute configuration of the above molecule using the Cahn-Ingold-Prelog convention. ii) Write the structure of the product that is formed when the above molecule is hydrogenated using H2 and palladium catalyst. Would the product be optically active? Explain.
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- Draw what would happen to 2,5-dimethyl-2-hexene in an alkyl halides and alkane reaction. This is for a concept map. So what would the alkene 2,5-dimethyl-2-hexene be as an alkyl halides and how to you go from an alkene to an alkane with 2,5-dimethyl-2-hexene. No bond lines. I know this much for alkene to alkaneIn each of the following classes of organic compounds, write (by express formula) two molecules each with at least one aromatic group and one alkyl group with a total of 10 carbons. Name each structure you write according to the IUPAC system. d) Write and name two diazonium salt.e) Write and name two 2,3-unsaturated aldehyde molecules.f) Write and name two corboxylic acid anhydride molecules.The instructions are to 1. list the functional group that differentiates benzhydrol from biphenyl 2. List the class of organic compound that differentiates benzhydrol from biphenyl. Would the answer for functional group be hydroxyl? I'm not sure about the class..?
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