Draw the products of this reaction. Jse a dash or wedge bond dicate the stereochemistry substituents on asymmetri centers. Ignore inorganic byproducts. J o
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- Rank the following groups in order of priority from highest (1) to lowest (3). < < -COO- -CH3 -NHCH3Pradet te major produet for he folewing trenatormation, e miedu of siereechamistry, when spplie Me. 1. ВНз THE 2. NaOH H2O2 H2O OA Oc OD. Me. OR HO Me OH Me- OH OH MePlease help with 4c, 4d, and 4e. We havent learned kaw of equivalents so please do 4c a different way. thank you
- K Draw one of the two diastereomers that are the major products from this reaction. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, Ignore inorganic byproducts. 1 Br2 Drawing V I I Probler Atom and || BrDraw a tetrahedral representation of the (2S,4S) enantiomer of 2-bromo-4-chlorohexane. O Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Show stereochemistry in a meso compound. [ ] در ? ChemDoodleⓇ6. Draw the stable conformations of the following molecules. A) (2R,3S)-3-methyl-2-hexanol (staggered Newman Projection). B) meso 1,2-dibromo cyclohexane in (chair conformation) 7. What is the value of the equilibrium constant for the following equilibrium? HC ECH + NaOH HC=C: Na + H₂O pk₂= 25 pka = 15.7
- Starting from the wedge-and-dash structure below (sighting down the indicated bond), rotate the back carbon to provide the structure in the conformation that will be capable of an E2 elimination. R/S stereochemistry is graded. # O H3C H Drawing > CI ||||| H Atoms, Bonds and Rings Tap a node to see sBuild a model of methylcyclohexane, and use the model to complete the following Newmanprojections of methylcyclohexane in the chair conformation: a. When the methyl group is in an axial or equatorial (circle one) position, the molecule is inits lowest potential energy conformation. b. Label one Newman projection above anti and the other gauche to describe the relationshipbetween the methyl group and C3 of the ring. c. In general, which is a lower PE conformation, anti or gauche? d. Explain how your answer to b and c provide an explanation for why it is more favorable fora large group to be in an equatorial than an axial position.+ CH2=CH' `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. L CONT. EXP. L C N CI Br Marvin JS [1] A by O ChemAxon P F -
- Draw the product of the reaction shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, Ignore inorganic byproducts. Illo. Av DrawingPart A || CH2=CH' 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. EXP. CONT. H +) C CI Br Marvin JS [1] by O ChemAxon F P.+ CH2=CH´ `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. EXP. CONT. .. C N CI Br Marvin JS [1] A by O ChemAxon P F