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My compound is 2,4-Dimethyl-1-Pentanol 1.       Retrosynthetic analysis of your compound: What is a possible precursor?   What are the...

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Chemistry

My compound is 2,4-Dimethyl-1-Pentanol

1.       Retrosynthetic analysis ofyour compound: What is a possible precursor?   What arethe reagents you need to obtain your product when using thisprecursor?     

2.       In a drawing, show thesynthetic steps that lead from the precursor to your compound. Usecurved arrows properly!

3.       Using your precursor, showmechanisms and products of a Markovnikov and an anti-Markovnikovaddition.

4.       Using the materials obtainedthrough Markovnikov and anti-Markovnikov additions to theprecursor, discuss stereochemical aspects. That means: Enantiomers?Diastereomers? Regioisomers? E. g., Markovnikovaddition yields the (?)-enantiomer, while …   . Are thecompounds chiral or achiral, why is that?

          Indicate theproper orientation of substituents by drawing structures withwedges and dashes where necessary.

5.         Identify allchiral centers in your substance and assign R- or S-designations.        

Answer & Explanation Solved by verified expert
4.0 Ratings (797 Votes)
1 Given below is a retrosynthetic analysis for24dimethyl2pentanol2 Shown below is a complete synthetic scheme for the formationof the    See Answer
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