D. these compounds in the boxes below. compounds D and E (both CsH10) that are geometric isomers of each other. Provide the structures of Compound A does not contain any chiral carbon atoms and reacts with concentrated H2SO4 to yield b) Assign letters to the three compounds you drew in part (a), as well as their reaction products, based on the following information: No IUPAC names are necessary. a) Provide the structures of these compounds in the boxes below. No IUPAC names are necessary. There are three structural isomers of formula CSH120 that contain a 2° alcohol. 4.

In addition to more highly fluorinated products, fluorination of 2-methylbutane yields a mixture of compounds with the formula C5H10F2. Draw the structures of all the isomers with the formula C5H10F2 that would be produced and label with a star all the chiral centers present in their structures.

Draw the line diagram structures of 5 compounds, each containing a different degree of unsaturation and a different functional group. Write the characteristic IR feature of each.

10. Provide a structure of an isomer that has the molecular formula C5H8O2 and fits the criteria described below. Note that all of the structures must be neutral and not have any formal charges on any of the atoms. a) Contains an ester and an alkene b) A chiral compound that contains a ring, ether and ketone. c) Contains an alcohol and an alkyne. d) A meso compound that contains two alcohols.

Give a brief answer to explain why acetic acid has a much higher BP (118 C) than 1- propanol (BP = 97 C) even though they both have the same size (molecular weight = 60) and they both form Hydrogen bonds.