The concept used to solve this problem is by using the given reagents, possible products will be formed in each step and then label it exactly in the given boxes in order to form the exact product.
Here, the starting reactant is ethyl benzene and the final product is (2-bromoethyl)benzene.
Bromine molecule is used for bromination of alkene. Trans addition takes place.
Addition of HBr to the double bond forms an alkyl bromide.
Potassium tertiary butoxide is a sterically hindered base.
Bromination of alkane in the presence of sunlight gives radical substitution.
NBS (N-bromosuccinimide) is used for the allylic bromination.
The reaction is as follows:
The reaction is as follows:
The reaction is as follows:
Ans:The best reagents that are used for the conversion of ethylbenzene to (2-bromoethyl)benzene are as follows:
Construct a multistep synthetic route from ethylbenzene to (2-bromoethyl)benzene by dragging the appropriate items into...
Construct a multistep synthetic route from ethylbenzene to (2-bromoethyl)benzene by dragging the appropriate items into the bins. Note that each bin will hold only one item, and not all reagents and structures will be used.
Construct a multistep synthetic route from ethylbenzene to (2-bromoethyl)benzene by dragging the appropriate items into the bins. Note that each bin will hold only oneitem, and not all reagents and structures will be used.
Several reagents and several organic structures are shown below. Construct a multistep synthetic route for the synthesis of acetylene from ethane by dragging the appropriate pieces into the bins. Note that each bin will hold only one item, and not every given reagent or structure will be used. (Stoichiometry is omitted.) Several reagents and several organic structures are shown below. Construct a multistep synthetic route for the synthesis of acetylene from ethane by dragging the appropriate pieces into the bins....
Several reagents and several organic structures are shown below. Construct a multistep synthetic route from the reactant 2-methyl-1-butene to the product 3-bromo-2-methyl-2-butanol by dragging the appropriate pieces into the bins. Note that each bin will hold only one item, and not every given reagent or structure will be used.
Several reagents and several organic structures are shown below. Construct a multistep synthetic route from the reactant 2-methyl-1-butene to the product 3-bromo-2-methyl-2-butanol by dragging the appropriate pieces into the bins. Note that each bin will hold only one item, and not every given reagent or structure will be used.
Several reagents and several organic structures are shown below. Construct a multistep synthetic route for the synthesis of acetylene from ethane by dragging the appropriate pieces into the bins. Note that each bin will hold only one item, and not every given reagent or structure will be used. (Stoichiometry is omitted.)
Several reagents and several organic structures are shown below. Construct a multistep synthetic route from the reactant 2-methyl-1-butene to the product 3-bromo-2-methyl-2-butanol by dragging the appropriate pieces into the bins. Note that each bin will hold only one item, and not every given reagent or structure will be used.
Several reagents and several organic structures are shown below. Construct a multistep synthetic route from the reactant 2-methyl-1-butene to the product 3-bromo-2-methyl-2-butanol by dragging the appropriate pieces into the bins. Note that each bin will hold only one item, and not every given reagent or structure will be used. HINT: Start by locating the structures of 2-methyl-1-butene and 3-bromo-2-methyl-2-butanol and placing them in their bins. Note that the final product is a vicinal halohydrin, since it has halogen and hydroxyl...
Answer with explanation please. Several reagents and several organic structures are shown below. Construct a multistep synthetic route from the reactant 2-methyl-1-butene to the product 3-bromo-2-methyl-2-butanol by dragging the appropriate pieces into the bins. Note that each bin will hold only one item, and not every given reagent or structure will be used.
Construct a three-step synthesis of 1,2-epoxycyclopentane from cyclopentanol by dragging the appropriate formulas into the bins. Note that each bin will hold only one item, and not all of the given reagents or structures will be used.