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- Draw the structures of the following molecules: (a) trans-l-Bromo-3-methylcyclohexane (b) cis-1, 2-Dimethylcyclobutane (c) trans-1 -tert-Butyl-2-ethylcyclohexaneName the following organic compound: CH3 S CH CH3 CH 0 CH, CH, 3-methylsulfide-2-ethoxy butane 2-ethoxy-3-methylthio butane O 3-ethoxy-2-methylthio butane O 2-methylsulfide-3-ethoxy butane O 2-ethoxy-3-methylsulfide butaneDraw the structural formula for each (i) 3-methyl-5-(2,2-dimethylpropyl) nonane(ii) 1,2-dichloro-3-methylcyclohexaneof the following compounds
- What is the name of the organic reactant and the resulting product of the reaction below? H H H H H H H-C-C-ċ=ċ-ċ-c-H + CI-CI H H H H O reactant: cis-3-hexene; product: 3,4-dichlorohexane reactant: trans-3-hexene; product: 3,4-dichlorohexane O reactant: cis-3-hexene product: 3,4-chlorohexane O reactant: cis-3-hexene product: dichlorohexaneMethyl isocyanate, CH3 -N= C = O, is used in the industrial synthesis of a type of pesticide and herbicide known as a carbamate. As a historical note, an industrial accident in Bhopal, India, in 1984 resulted in leakage of an unknown quantity of this chemical into the air. An estimated 200,000 people were exposed to its vapors, and over 2000 of these people died. Q.) Methyl isocyanate reacts with strong acids, such as sulfuric acid, to form a cation. Will this molecule undergo protonation more readily on its oxygen or nitrogen atom? In considering contributing structures to each hybrid, do not consider structures in which more than one atom has an incomplete octetDraw the structure of the following compounds (E)-3,7-Dimethyloct-3-ene and Neopentylcyclohexane
- Draw the constitutional isomer formed when the following alkenes are treated with each set of reagents: [1] H2O, H2SO4; or [2] BH3 followed by H2O2, −OH.Which of the following is a correct IUPAC name for the molecule shown. CH, H3C CH,CH,CH2 CH3 O (2E, 4Z)-4,5-dimethyloctadiene O (2E, 4E)-4,5-dimethyloctene • (2E, 4E)-4,5-dimethyloctadiene o (4E, 6E)-4,5-dimethyloctadiene (22, 4Z)-4,5-dimethyloctadieneWhat is the IUPAC name of the following molecule? s O 1-cyclohexyl-1,3,4-trimethyl-(1Z,3E)-1,3-hexadiene 6-cyclohexyl-3,4,6-trimethyl-(3E,5Z)-3,5-hexadiene O 6-cyclohexyl-3,4,6-trimethyl-(3Z,5E)-3,5-hexadiene 1-cyclohexyl-1,3,4-trimethyl-(1E,3Z)-1,3-hexadiene
- How many alkenes or cycloalkenes with the general formula C9H16 can you treat with HCl to obtain 1-chloro-1-ethyl-3,4-dimethylcyclopentane as a major product?Compounds A and B are isomers of the molecular formula CyH19Br. Both yield the same alkene Cin an elimination reaction. Hydrogenation of C yields the product 2,3,3,4 tetramethyl pentane. What are the structures of A, B, and C?Draw the constitutional isomer formed when the attached alkenes are treated with each set of reagents: [1] H2O, H2SO4; or [2] BH3 followed by H2O2, −OH.