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6. Synthesis: (40 pts) Show how you would carry out the following synthesis using inorganic or...
6. Synthesis: (40 pts) Show how you would carry out the following synthesis using inorganic or organic reagents containing four or less carbons. Include the reagents you would need for each step and the structure of the intermediate products formed in each step in the appropriate boxes. CI A) Cyclobutane 1) 2) 1) 2) Br B) OH 1) 2)
6. Synthesis: (40 pts) Show how you would carry out the following synthesis using inorganic or organic reagents containing four or less carbons. Include the reagents you would need for each step and the structure of the intermediate products formed in each step in the appropriate boxes. CI A) Cyclobutane 1) 2) 1) 2) Br B) OH 1) 2)
6. Synthesis: (40 pts) Show how you would carry out the following synthesis using inorganic or organic reagents containing four or less carbons. Include the reagents you would need for each step and the structure of the intermediate products formed in each step in the appropriate boxes. CI The product should be chloro-3-methylhexane A) Cyclobutane 1) -> 2) 1) 2) Br O B) OH 1) 2)
6. Synthesis: (40 pts) Show how you would carry out the following synthesis using inorganic or organic reagents containing four or less carbons. Include the reagents you would need for each step and the structure of the intermediate products formed in each step in the appropriate boxes. CI A) Cyclobutane 1) 2) 1) 2) Br B) ОН 1) 2)
6. Synthesis: (40 pts) Show how you would carry out the following synthesis using inorganic or organic reagents containing four or less carbons. Include the reagents you would need for each step and the structure of the intermediate products formed in each step in the appropriate boxes. Cyclobutane 1) 2) 1) 2) Br B) OH 1) 2)
6. Synthesis: (40 pts) Show how you would carry out the following synthesis using inorganic or organic reagents containing four or less carbons. Include the reagents you would need for each step and the structure of the intermediate products formed in each step in the appropriate boxes. A) Cyclobutane 1) 1) 2) Br 0 B) OH 1) 2)
6. Synthesis: (40 pts) Show how you would carry out the following synthesis using inorganic or organic reagents containing four or less carbons. Include the reagents you would need for each step and the structure of the intermediate products formed in each step in the appropriate boxes. CI * A) Cyclobutane 1) 2) 1) 2)
6. Synthesis: (40 pts) Show how you would carry out the following synthesis using inorganic or organic reagents containing four or less carbons. Include the reagents you would need for each step and the structure of the intermediate products formed in each step in the appropriate boxes. Br B) ОН 1) 2) —
IT IS AN ORGANIC CHEMISTRY SYNTHESIS QUESTION 6. Synthesis: (40 pts) Show how you would carry out the following synthesis using inorganic or organic reagents containing four or less carbons. Include the reagents you would need for each step and the structure of the intermediate products formed in each step in the appropriate boxes. CI The product should be 3-chloro-3-methylhexane A) Cyclobutane 1) 2) 1) 2) como B) OH 1) 2)
94 7. Spectroscopy: (20 pts) The unknown compound A (C17H3403) gives the following 'H NMR and IR spectra. Include degrees of unsaturation and show your work for partial credit. What is the structure of compound A? 6H 4H 2H 2H IH IH 24 24 24 24 1ң With the heat 5 4 دیا 2 M Lumm mm 4000 3000 2000 1000 500 1500 Wavenumbers 6. Synthesis: (40 pts) Show how you would carry out the following synthesis using inorganic or...