Compounds X, C9H19Br, and Y, C9H19Cl, undergo base-promoted E2 elimination to give the same single alkene product, Z. Catalytic hydrogenation of Z affords 2,3,3-trimethylhexane. In water X readily reacts to give a substitution product, C9H19OH, together with Z. Y does not react with water. Propose structures for X and Y.

Look at the reaction below: ca(hco3)2 --> caco3 + co2 + h2o first, balance the reaction. once balanced, use dimensional analysis or another method to find out how many moles of carbon dioxide will be produced if we start with 16.5 moles of calcium bicarbonate (calcium hydrogen carbonate). = mol of co2 number needs to be reported to three significant figures.

Draw the structure for 5-isopropyl-2-methyl-3-nonene

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