Video Solution: Suggest a sequence of reactions suitable for preparing each ...

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Suggest a sequence of reactions suitable for preparing each of the following compounds from the indicated starting material. You may use any necessary organic or inorganic reagents. 

(h) tert -Butyl iodide from isobutyl iodide 

Provide the reagents necessary to make the indicated product from the indicated starting materials; more than one step maybe necessary.

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Propose an efficient method of converting 3-methyl-1-butanol into 3-methyl-2-butanol.

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Provide a curved arrow mechanism for the following reaction.

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Provide an efficient multistep synthesis for the conversion of the given starting material into the target molecule shown to the right. You must begin with the given starting organic compound. All Cs that  end up in the target compound must come from the given starting organic compound. For each functional group transformation, give all necessary reagents, solvents, and catalysts; give a structural formula for each organic reactant and the major organic product(s). Show stereochemistry appropriately when necessary. If a mixture of products (for example a mixture of stereoisomers) must be present after a step, assume that you can separate the mixture and take the one needed product forward through the next step.

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Propose a synthetic way to produce the following compound.

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Propose a synthetic way to produce the following compound.

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Propose a synthetic way to produce the following compound.

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Show how you would carry out each of the following reactions. You do   NOT need to draw the mechanisms

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Show how you would carry out each of the following reactions. You do   NOT need to draw the mechanisms 

 

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Provide an efficient multistep synthesis for the following conversion of the given starting compound into the target compound. For this problem, do not give a mechanism with curved arrows. For the synthesis, more than one functional group transformation is required. For each functional group transformation, give all necessary reagents and catalysts and give a structural formula of the organic product. Also give hv and/or heat when necessary. Show stereochemistry appropriately when necessary. 

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Fill in the missing reagents:

 

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