Questions from Organic Chemistry

Q: Starting with 4-nitrostyrene and using any other reagents of your

Starting with 4-nitrostyrene and using any other reagents of your choice, show how you would make each of the following:

Q: Propose a two-step synthesis that will achieve the following transformation

Propose a two-step synthesis that will achieve the following transformation:

Q: Using 1-pentene as your only source of carbon atoms,

Using 1-pentene as your only source of carbon atoms, show how you would use a Corey–Posner/Whitesides–House reaction to prepare decane.

Q: Starting with benzene and any other reagents of your choice, propose

Starting with benzene and any other reagents of your choice, propose a synthesis for each of the following compounds:

Q: Predict the major product for each of the following transformations and propose

Predict the major product for each of the following transformations and propose a mechanism for its formation:

Q: Starting with diethyl malonate and using any other reagents of your choice

Starting with diethyl malonate and using any other reagents of your choice, show how you would prepare each of the following compounds:

Q: The following compound will undergo an intramolecular Heck reaction to give a

The following compound will undergo an intramolecular Heck reaction to give a single product with two chiral centers. This process is observed to occur diastereoselectively (a new chiral center is for...

Q: Starting with cyclopentene and using any other reagents of your choice,

Starting with cyclopentene and using any other reagents of your choice, show how you would make each of the following compounds:

Q: When treated with a Grubbs catalyst, compound A (under conditions

When treated with a Grubbs catalyst, compound A (under conditions of high dilution) is converted into one product (compound 1) with the molecular formula C6H8O2. Under similar conditions, compound B i...

Q: When a Stille coupling reaction is performed in the presence of carbon

When a Stille coupling reaction is performed in the presence of carbon monoxide (CO), a ketone is obtained, as shown here: Using this procedure, show how you would make each of the following compound...