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Consider the reaction coordinate diagram shown.  Choose the correct statement about step 1.

Examine the structure of the molecule below.  What intermolecular forces should it have in liquid form? Choose all that apply.  

In lab, you performed an acid-base extraction and then neutralization to isolate aspirin. Choose the product of the reaction as indicated:

Examine the structure of the molecule below.  What intermolecular forces should it have in liquid form? Choose all that apply.  

Choose the correct line structure for the formula HOOCCH2CH(NH2)COOH.

The optical rotation of (R)-carvone is -61 o .  What would be the optical rotation of a racemic mixture of carvone, 50% of (R)-carvone and (S)-carvone ?

Consider the reaction coordinate diagram shown. Which step has the lowest rate constant in the forward direction (in other words, which step is the slowest)?

Choose all molecules below that are achiral.  

Which orbitals are used to form the sigma bond between carbons 1 and 2 below.

Choose the most correct resonance form for the following structure and arrows.