How can we convert 1-hexene to cis-3-octene using alkynes as intermediates?

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To convert 1-hexene to cis-3-octene using alkynes as intermediates, the process involves first transforming the alkene into an alkyne. This can be achieved by removing hydrogens from the double bond, followed by the addition of a methyl group to the terminal carbon, potentially using CH3-Br for substitution. The synthesis requires careful consideration of maintaining the double bond's position while introducing the new alkyl group. The discussion emphasizes the need for a strategic approach to ensure the correct stereochemistry and structure of the final product. Overall, the synthesis pathway hinges on effective manipulation of the alkyne and alkene functionalities.
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Organic: Alkene to Alkyne

I am trying to do a synthesis of 2-Octyne from 1-heptene. Conversion of the triple bond to a double bond is pretty easy, but i also have to add an alkyl group, and the double bond must remain on the original triple bond location.

Thus, so far thoughts:
1. remove hydrogens from double bond

2. add ch3 to terminal carbon to replace hydrogen.
CH3-BR ?

Question 2: Propose a synthesis of cis-3-octene starting from 1-hexene.
 
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You need to review the http://courses.chem.indiana.edu/c341/documents/C341S2010CH7Alkynes.pdf"
 
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