Answer:
The reagents for forward synthesis of styrene from benzene is
1. H. AcCl, AlCl3, THF, 65oC
2. V. NaBH4, EtOH, 25oC
3. X. H2SO4, H2O, 100oC
QUESTION 9 Using the list, propose the forward synthesis of the retrosynthesis shown below (and number...
Using the list, propose the forward synthesis of the retrosynthesis shown below (and number of steps can be used, so long as they get to the desired product in as high a regioselectivity as possible). Please report your answer by typing the letters/symbols sequentially. A. Ph3PMeBr, KotBu, PhMe, 25 °C B. CuBr, 0 °C C. Cu20, Cu(NO3)2, H20, 0 °C D. CuCN, 0 °C E. SO3, H2SO4, 100 °C F. Cl2, FeCl3, THF, 65 °C G. Br2, FeBr3, THF, 65...
Using the list, propose the forward synthesis of the retrosynthesis shown below (and number of steps can be used, so long as they get to the desired product in as high a regioselectivity as possible). Please report your answer by typing the letters/symbols sequentially. Using the list, propose the forward synthesis of the retrosynthesis shown below (any number of steps can be used, so long as they get to the desired product in as high a regioselectivity as possible). Please...
Using the list, propose the forward synthesis of the retrosynthesis shown below (and number of steps can be used, so long as they get to the desired product in as high a regioselectivity as possible). Please report your answer by typing the letters/symbols sequentially. QUESTION 9 Using the list, propose the forward synthesis of the retrosynthesis shown below (and number of steps can be used, so long as they get to the desired product in as high a regioselectivity as...
Using the list, propose the forward synthesis of the retrosynthesis shown below (any number of steps can be used, so long as they get to the desired product in as high a regioselectivity as possible). Please report your answer by typing the letters/symbols sequentially. Оме Meo Оме Meo Meo A. Ph3PMeBr, KotBu, PhMe, 25 °C B. CuBr, 0 °C C. Cu20, Cu(NO3)2, H20, 0 °C D. CuCN, 0 °C E. SO3, H2SO4, 100 °C F. Cl2, FeCl3, THF, 65 °C...
QUESTIONS Using the list, propose the forward synthesis of the retrosynthesis shown below any number of steps can be used, so long as they get to the desired product in as high a regioselectivity as possible). Please report your answer by typing the letterssymbols sequentialy НО. ana OH A. CUCI, 0 °C B. CuBr, 0 °C C. Cu20, Cu(NO3)2, H20, 0 °C D. EuCN, 0 °C E. SO3, H2SO4, 100 °C F. Cl2, FeCl3, THF, 65 °C G. Bre, FeBr3,...
Using the list, propose the forward synthesis of the retrosynthesis shown below (any number of steps can be used, so long as they get to the desired product in as high a regioselectivity as possible). Please report your answer by typing the letters/symbols sequentially. QUESTION 8 Using the list, propose the forward synthesis of the retrosynthesis shown below (any number of steps can be used, so long as they get to the desired product in as high a regioselectivity as...
Using the list, propose the forward synthesis of the retrosynthesis shown below (and number of steps can be used, so long as they get to the desired product in as high a regioselectivity as possible). Please report your answer by typing the letters/symbols sequentially, A. PH. Br, KotBu, PhMe, 25 °C L. NaOH, H20, 160 °C B. CuBr 0 °C M. H2O, Dilute H2SO4, 100°C C. Cu20, Cu(NO3)2, H20.0°C N. HNO3, H2SO4, 60 °C D. CuCN, 0 °C E. SO3,...
Using the list, propose the forward synthesis of the retrosynthesis shown below (any number of steps can be used, so long as they get to the desired product in as high a regioselectivity as possible). Please report your answer by typing the letters/symbols sequentially. НО. OH A. CUCI, 0 °C B. CuBr, 0 °C C. Cu20, Cu(NO3)2, H20, 0 °C D. CuCN, 0 °C E. SO3, H2SO4, 100 °C F. Cl2, FeCl3, THF, 65 °C G. Br2, FeBr3, THF, 65...
Using the list, propose the forward synthesis of the retrosynthesis shown below (and number of steps can be used, so long as they get to the desired product in as high a regioselectivity as possible). Please report your answer by typing the letters/symbols sequentially OMe Meo CI Meo Meo A. Ph3PMeBr, KotBu, PhMe, 25 °C B. CuBr 0 °C C. Cuyo, Cu(NO3)2, H20.0°C D. CuCN, 0 °C E. SO3, H2SO4. 100 °C F. Cl2, FeCl3, THF, 65 °C G. Brz,...
Using the list, propose the forward synthesis of the retrosynthesis shown below (and number of steps can be used, so long as they get to the desired product in as high a regioselectivity as possible). Please report your answer by typing the letters/symbols sequentially HO ОН A. CUCI, B. CuBr. 0 °C C. Cu20, Cu(NO3)2, H20.0°C D. CuCN. 0 °C E. SO3, H2SO4, 100 °C F. Cl2, FeCl3, THF, 65 °C G. Br2, FeBrz. THF, 65 °C H. ACCI, AICI3....