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- 3.provide the starting materials needed to synthesize each compound.Complete the flowchart by drawing the resulting structures of each reaction. A. B. C. D. E. F. G. H. I.[VII4,5] Instructions: Answer the following: (Refer to the photo below) 4. What is the structure of compound C? 5. What is the structure of compound A?
- Identify the reagents a-c in the following scheme:Under certain reaction conditions, 2,3-dibromobutane reacts with twoequivalents of base to give three products, each of which contains twonew π bonds. Product A has two sp hybridized carbon atoms, product Bhas one sp hybridized carbon atom, and product C has none. What arethe structures of A, B, and C?Bicyclo[2.2.1]heptan-7-one + PCC (in CH₂Cl₂) => A.) Bicyclo[2.2.1]heptan-7-ol B.) Bicyclo[2.2.1]heptanoic acid C.) Cyclohexanecarbaldehyde D.) All the given choices are possible products E.) No reaction
- What is the major product of the following reaction? A B C DTreatment of compound A (C8H17Br) with NaOCH2CH3 affords two constitutional isomers B and C. Ozonolysis of B affords CH2=O and (CH3CH2CH2)2C=O. Ozonolysis of C affords CH3CH2CH2COCH3 and CH3CH2CHO. What is the structure of A?Treatment of compound A (C8H17Br) with NaOCH2CH3 affords twoconstitutional isomers B and C. Ozonolysis of B affords CH2=O and(CH3CH2CH2)2C=O. Ozonolysis of C affords CH3CH2CH2COCH3 andCH3CH2CHO. What is the structure of A?
- Draw the product obtained when cis-2-butene is treated first with Br2 in CH2Cl2, second with NaNH2 in NH3, and then finally with Li in NH3.An allylic alcohol contains an OH group on a carbon atom adjacent to a C—C double bond. Treatment of allylic alcohol A with HCl forms a mixture of two allylic chlorides, B and C. Draw a stepwise mechanism that illustrates how both products are formed.An allylic alcohol contains an OH group on a carbon atom adjacent to a C − C double bond. Treatment of allylic alcohol A with HCl forms a mixture of two allylic chlorides, B and C. Draw a stepwise mechanism that illustrates how both products are formed.