Write bond-line formulas for four carboxylic acids with the formula C5H1002. Write bond-line formulas for three esters with the formula CSH1002.

Draw Lewis structures and condensed structural formulas for the four alcohols with the molecular formula C4H10O. Classify each alcohol as primary, secondary, or tertiary. (Hint: First consider the connectivity of the four carbon atoms; they can be bonded either four in a chain or three in a chain with the fourth carbon as a branch on the middle carbon. Then consider the points at which the iOH group can be bonded to each carbon chain.)

Draw Lewis structures and condensed structural formulas for the two alcohols with the molecular formula C3H8O. Classify each as primary, secondary, or tertiary.

12. Write bond-line structural formulas for (a.) two primary alcohols, (b.) a secondary alcohol, and (c.) a tertiary alcohol-all having the molecular formula CaH100.

Draw the Lewis structure for an isomer of C3H6O that is a ketone, and draw another Lewis structure for an isomer of C3H6O that is an aldehyde.

In what way(s) is(are) the structure of H2O similar to that of CHCl3? In what way is the structure of water different from that of CHCl3?

What are the hybridization and bond angles of the oxygens in benzoic acid?

Compounds Y and Z both have the formula C₂H18. Both Y and Z react with one molar equivalent of hydrogen in the presence of a palladium catalyst to form 2-methyloctane. The heat of hydrogenation of Y is less than that of Z. Y and Z each undergo hydroboration/oxidation to give a primary alcohol (OH attached to a primary carbon). What is the structure of Y? • In cases where there is more than one answer, just draw one. 1998) 0▾ + n [F ChemDoodle a

Find the butanol combustion enthalpy using bond energy  and calculate the value of the change in heat of combustion due to the addition of a CH2 unit in the given alcohol

Write the structural formula for 3-methylcyclohexanol.