3. Draw all the products, including all stereoisomers that form when the optically active compound below reacts wit...
A compound has the chemical formula CaH1oO and it is optically active. The compound reacts with HCl and ZnCl2 (the so-called Lucas test) to form a cloudy product within 10 minutes. What is the structure of the compound?
help Thank you 4. (10 pts) Draw all possible products for the following reaction including stereoisomers. Note that the addition occurs through a "syn" mechanism. Is the product solution optically active (yes or no)? 1. BAHATHF 2. NaOH, HO (8 pts) Provide a complete mechanism for the reaction below and include lone-pairs of electrons and formal charges. Show all products formed including stereoisomers. Is the product solution optically active (yes or no)? Bras 11. (8 pts) Draw all four regiochemical...
2. Draw the major product(s) formed when the optically active compound shown below is treated with H2O/H2SO4. Is the product optically active? Why or why not? (4 pts) optically active
Draw the unique stereoisomers for 1,2-difluorocyclohexane. Show stereochemistry clearly. To ensure proper grading, explicitly draw all four groups, including wedge/dash bonds, around a chirality center. Indicate whether the compound(s) could exist in an optically active form.
Draw the structure of the products formed when the sugar below is reacted with sodium borohydride followed by water. On the lines provided, indicate whether each product is optically active (O.A.) or optically inactive (O.I.).Show the mechanism.
2) a) Consider 2-bromo-3-chlorobutane. How many stereoisomers are possible for this compound? Draw all stereoisomers, label each stereocenter with the appropriate R/S designation to show handedness, and indicate the relationship (enantiomers or diastereomers) between every possible pairing of compounds. Name each compound according to IUPAC nomenclature, using appropriate R/S designation to show handedness. b) Repeat this exercise for 2,3-Butanediol. What is different about this compound relative to the first example? What word describes the unique stereoisomer? c) Which of the...
Draw the unique stereoisomers for 2-chloro-2,3-dimethylpentane. Show stereochemistry clearly. To ensure proper grading, explicitly draw all four groups, including wedge/dash bonds, around a chirality center. Indicate whether the compounds could exist in an optically active form.
Which of the following substances can exist in an optically active form? Draw structures, and locate with an asterisk all chiral centers in each a. 2-methylbutane b. 1,2,3,4-tetrachloropentane
Part A Draw all the products formed when the compound shown below undergoes reaction with HCI. Interactive 3D display mode Hgc -CH3 Draw the molecules on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default. Show the appropriate stereochemistry by choosing the dashed or wedged buttons and then clicking a bond on the canvas. 02 H+ 200 mm Co +
Draw the correct structure(s) for cis-1-bromo-3-methylcyclohexane. Show stereochemistry clearly. To ensureproper grading, explicitly draw all four groups, including wedge/dash bonds, around a chirality center. Indicate whether the compound(s) could exist in an optically active form. could exist in optically active form cannot exist in optically active form cannot be determined