Chapter 12: Q.67. (page 493)
Question:Devise a synthesis of 1-phenyl-5-methylhexane from acetylene, alkylhalides, and any required inorganic reagents.
Short Answer
Answer
Chapter 12: Q.67. (page 493)
Question:Devise a synthesis of 1-phenyl-5-methylhexane from acetylene, alkylhalides, and any required inorganic reagents.
Answer
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Get started for freeQuestion: A chiral alkyne A with molecular formula C6H10 is reduced with and Lindlar catalyst to B having the R configuration at its stereogeniccentre. What are the structures of A and B?
Question: a) Draw the structure of a compound of molecular formula C6H10 that reacts with H2 in the presence of Pd-C but does not react with H2in the presence of Lindlar catalyst. (b) Draw the structure of a compound of molecular formula C6H10 that reacts with H2 when either catalyst is present
Question:Devise a synthesis of each compound from acetylene and any other required reagents.
Question: An unknown compound A of molecular formula reacts with to form two compounds (B and C) of molecular formula . B and C both react with in the presence of Pd-C to form decalin. Ozonolysis of B forms D, and ozonolysis of C forms a diketone E of molecular formula . Identify the structures of compounds A, B, C and E.
Question: Epoxidation of the following allylic alcohol using the Sharpess reagent (-)-DET gives two epoxy alcohols in a ratio of 87:13.
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