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Alkynide Retrosynthesis Solutions Library

Access 11 Alkynide Retrosynthesis video and text solutions to help you complete your homework.

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11 solutions

Alkynide Retrosynthesis

Q. What reagents can be used to form the alkyne product shown from acetylene? Select all necessary reagentsCH3l CH3CH2l NaOH CH3CH2CH2lNaH

Solved • May 24, 2018

Alkynide Retrosynthesis

Q. Working backwards, deduce the starting material that led to the indicated product through the defined reactions. Draw the reagent A of the followin...

Solved • May 24, 2018

Alkynide Retrosynthesis

Q. What is the starting material that affords the following product in the highest yield? 1.1-dibromopentane 1.2-dichloropent-1 -ene 1.1-dichlorobutan...

Solved • May 11, 2018

Alkynide Retrosynthesis

Q. Provide the reagent or starting material to perform the indicated transformation. More than one reaction may be required. You should number your st...

Solved • Jun 9, 2017

Alkynide Retrosynthesis

Q. Prepare the compound shown below from acetylene.    

Solved • May 8, 2017

Alkynide Retrosynthesis

Q. Show how you would perform the following transformation.

Solved • Mar 27, 2017

Alkynide Retrosynthesis

Q. Provide the reagents required for the following transformations. Note, that some of these methods will require more than one chemical step. All the...

Solved • Aug 2, 2016

Alkynide Retrosynthesis

Q. Draw the starting material that, under the given reaction conditions, results in the following products.

Solved • Jul 27, 2016

Alkynide Retrosynthesis

Q. Alkene derivatives of pristine (2,6,10,14-tetramethylpentadecane) can be isolated from marine zooplankton and are important in the study of the mar...

Solved • Apr 25, 2016

Alkynide Retrosynthesis

Q. Propose a mechanism for the following reaction. Include all reagents and intermediates.

Solved • Mar 14, 2016

Alkynide Retrosynthesis

Q. A number of drugs are prepared by reactions in which carbon-carbon bond formation is the last step. Indicate what you believe would be a reasonable...

Solved • Feb 11, 2016