During clinical trials it was discovered that smokers, after one to two weeks on the drug, reported that their craving for tobacco had lessened. Further sudies confirmed this finding and the drug is now marketed under the name Zyban as an aid in smoking cessation. Propose a synthesis of bupropion from benzene. ols CI From the table of reagents, select the components necessary to synthesize the given molecule and enter their letters, in the order that they are to be used without commas between, in the box, i.e. 'hiacc'. If a reaction is to be used more than once, enter its letter multiple times as necessary. Reagents Available a. CH3CH=CH2, H3PO4 b. acetyl chloride, AlCl3 c. HNO3/H₂SO4 d. 2-methylpropanoyl chloride, AlCl3 e. H₂, Pd/C f. BH3/THF g. H₂NNH₂, OH, H₂O h. OH- i. CH31 j. H₂CRO4 k. Br₂, FeBr3 I. SOCI₂ m. Cl₂, FeCl3 n. Cl₂, A o. propanoyl chloride, AICI3 p. Br₂, H+ q. t-butylamine Previous Next
Carbohydrates
Carbohydrates are the organic compounds that are obtained in foods and living matters in the shape of sugars, cellulose, and starch. The general formula of carbohydrates is Cn(H2O)2. The ratio of H and O present in carbohydrates is identical to water.
Starch
Starch is a polysaccharide carbohydrate that belongs to the category of polysaccharide carbohydrates.
Mutarotation
The rotation of a particular structure of the chiral compound because of the epimerization is called mutarotation. It is the repercussion of the ring chain tautomerism. In terms of glucose, this can be defined as the modification in the equilibrium of the α- and β- glucose anomers upon its dissolution in the solvent water. This process is usually seen in the chemistry of carbohydrates.
L Sugar
A chemical compound that is represented with a molecular formula C6H12O6 is called L-(-) sugar. At the carbon’s 5th position, the hydroxyl group is placed to the compound’s left and therefore the sugar is represented as L(-)-sugar. It is capable of rotating the polarized light’s plane in the direction anticlockwise. L isomers are one of the 2 isomers formed by the configurational stereochemistry of the carbohydrates.
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