(R)-limonene is found in many citrus fruits, including oranges and lemons. Identify where are their chiral center located and how many groups each has, then assign priorities from the lowest 4 to the highest which is 1.
(R)-limonene is found in many citrus fruits, including oranges and lemons. Identify where are their chiral center locate...
5.50 S= 61XLUI (R)-Limonene is found in many citrus fruits, including oranges and lemons For each of the following compounds identify whether it is (R)-limonene or its enantion limonene: (a)
5.50 (R)-Limonene is found in many citrus fruits, including oranges and lemons: pd For each of the following compounds identify whether it is (R)-limonene or its enantiomer, (S) limonene: wollo sd To s (a) lid (b) (c) (d)
153 (R)-Limonene is found in many citrus fruits, including oranges and lemons: Draw the structures and identify the relationship of the two products btained when (R)-Limonene is treated with excess hydrogen in the esence of a catalyst.
4,5,6 4. (1 pt.) Name the following compounds. Assign R S for chiral center and use E Z to describe double bond. 5. (1 pt.) How many tetrahedral stereocenters (chiral centers) are there in the molecule shown below. Mark each one with an asterisk. B. How many configurational isomers total are possible for this structure? A Number of tetrahedral stereocenters B. Total number of configurational isomers 6. (1 pt.) Identify all molecules that are chiral and the ones that are...
Which of the compounds shown below are chiral? (choose all correct) ОН o ОН E Which of the compounds shown below is/are chiral? (choose all correct answers) O For determining whether a stereogenic center is Ror S. the substituents need to be ranked. Rank the following substituents from high to low, entering a 1,2,3, or 4 next to each structure, with 1 for highest priority ranking and 4 for lowest priority ranking. 0-6 -C-H -CH_Br -CH₂OH -c-oh Which of the...
6. Draw the structure of Compound Y 1. O 2. Zn, H3O 7. Draw all resonance contributors to this species: CHz 8. a) State the hybridization (sp, sp2, sp) of each carbon in this compound, going left to right. b) Write "highest under the compound which is in the highest oxidation state. Write "lowest" under the compound which is in the lowest oxidation state. CH2Cl2 CH4 9. a) Write out seven separate reactions of 2-methyl-2-butene, including reagent(s) and products(s). Include...
6. Draw the structure of Compound Y Compound YCH,CCH2CH2CH2CH 2. Zn, H3O 7. Draw all resonance contributors to this species: CH2 8. a) State the hybridization (sp3, sp, sp) of each carbon in this compound, going left to right b) Write "highest" under the compound which is in the highest oxidation state. Write "lowest" under the compound which is in the lowest oxidation state. CH2Cl2 O-C O CH4 9. a) Write out seven separate reactions of 2-methy -2-butene, including reagent(s)...
Solve 12-14 12. Consider the molecule shown below. OH OH f. How many stereoisomers are possible? g. Draw each of these stereoisomers. h. Identify pairs of enantiomers and pairs of diastereomers. i. Build a model of the stereoisomer that has both OH groups pointing out. Also, build a model of the mirror image of this molecule. j. Do your two molecules represent enantiomers? Are they chiral? Fischer Projections 13. Build a model of 1-bromo-1-chloroethane. a. Draw a3D representation of this...
rojection Formulas for each model in #16 (again orient the carbon chain up and down). Are the mirror images "superimposable?" Interchange any two of the groups located at one of the chiral centers on one of the models in # 1 6. What is the stereochemical relationship of the resulting structure with the one that used to be its mirror image? Will this 'new' model be "optically active?" Why or why not? 18. PART 4:2,3-DICHLOROPENTANE CH, CH(C)-CHC)-CH2CH Build a model...
19-26 thanks! 19-29* PART 3: 2,3-BUTANEDIOL CH-CH(OH)-CH(OH)-CH, mirror images, not superimposable Build as many models of 2,3-butanediol as you can. First, attach two carbons with a single bond. To each carbon add one carbon, one hydrogen, and one oxygen. To complete the structure, Ti the remaining hydrogen atoms. Remember, a model is not different if it is completely superimposable on one already constructed! 13. How many stereochemically different models are possible for 2,3-butanediol? 14. What characteristic does one of these...