Draw a bondline representation of s-2-chloro-2-fluorobutane?
based on the name we draw the structure
Draw (2R)-2-chloro-2-butanol and (2S)-2-chloro-2 butanol in 3D (
wedges and dashes shown clearly)
Ciastereomer 2. Draw (2R)-2-chloro-2-butanol and (2S)-2-chloro-2-butanol in 3D format (wedge and dashes shown clearly) CI, OH Ev & DH 2-chloro-2-butanol
1. Draw the structure of 4-chloro-2-methylcyclohexanol. 2. Draw the structure of 3-chloro-2-iodo-N,N-dimethylaniline. 3. Draw the structure of the products of the basic hydrolysis of 2-propyl pentanoate using sodium hydroxide.
Draw the mechanism and the product(s)for the acid-catalyzed reaction of (S)-4-chloro 2-pentanone with 2 moles of methanol; indicate which is the hemiacetal and the acetal structures. Consider how would the mechanism and the product be different if the same ketone underwent acid hydrolysis in the absence of methanol? Also, consider the reversibility of the above mechanisms.
2. (4 pts) Draw the structures of the two possible products- 3-chloro-1-butene and 1-chloro-2- butene. What type of isomers are these two compounds?
Draw structures for the following compounds. a. 2-chloro-1,3-cyclopentadiene b. 2-bromo-5-nitroaniline c. 2-chloro-5-fluoro-3-octyne
Draw the substitution product of the reaction of (1 S,3R)-1-chloro-3-methylcyclohexane with hydroxide.
1. Below is a sawhorse representation of 1-chloro-1-fluoropropane. Construct an energy diagram describing rotation about the C1-C2 bond (shown in red). Draw Newman projections for the 6 limiting conformations. Remember, the larger the substituent, the repulsion between it and other groups. Here, the size increases in the order H F < Cl CH3 more CH3 H H H CI
(R)-2-chloro-(S)-3-bromobutane and (S)-2-chloro-(S)-3-bromobutane are: A. enantiomers. B. diastereomers. C. meso compounds. D. the same molecule.
1) Draw structures for compounds named below. A) (Z)-1-bromo-2-chloro-1-heptene B) 4-chloro-4-fluoro-2-octyne
5. Draw 2-chloro-3,3-dimethylheptane in the space provided below: