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How would you describe the molecule below? ОН HO ОН sp hybridized Cis Trans Optically active
The molecule below is: ОН ОН Optically active Non superimposible on its mirror image Both (-)...
The molecule below is: ОН ОН Optically active Non superimposible on its mirror image Both (-) and (+) Achiral
20. Make a model of trans-1, 4-dimethylcyclohexane and cis-1, 4-dimethylcyclohexane. Draw their chair conformations below including...
20. Make a model of trans-1, 4-dimethylcyclohexane and cis-1, 4-dimethylcyclohexane. Draw their chair conformations below including the chair flip for each. Repeat questions 15-16 on this model Part III. Learning to Draw Molecules on a Computer Start the ACD ChemSketch programs and spend 15 minutes familiarizing yourself with their drawing capabilities. Practice using ChemSketch 2.0 to convert two dimensional structures to three dimensional structures and rotating and viewing three dimensional structures. 1. Based on the shape of the molecule, what...
please answer all Question 1 2 pts Determine whether the molecule below is optically active. cannot...
please answer all
Question 1 2 pts Determine whether the molecule below is optically active. cannot determine O optically active O optically inactive Question 2 2 pts Determine the relationship between the two molecules below NH2 HO H3COOH identical enantiomers constitutional isomers diastereomers Question 3 2 pts Determine the relationship between the two molecules below H HOW enantiomers O identical constitutional isomers diastereomers D Question 4 2 pts Determine the total number of stereoisomers represented by the bond line drawing...
6 CHM 2440 (FA 2019) Sp hybridized atoms has a trigonal planar geometry of their hybridized...
6 CHM 2440 (FA 2019) Sp hybridized atoms has a trigonal planar geometry of their hybridized orbitals. This will affect the geometry of the molecule- wben covalent bonds are formed, it makes the neighboring atoms coplanar. For example: CH,-CH, is a planar structure with both carbon and all four hydrogen atoms on the same plane. HiH Circle the carbon atoms that are co-planar in the structure below. (0.25 pt) CH3 H3C-CH2-C CH2-CH3 5. Give the IUPAC name for each of...
7. (9 pts) (Are the following optically active or meso? meso HyCHC OH HO opticaly actve...
7. (9 pts) (Are the following optically active or meso? meso HyCHC OH HO opticaly actve active opti call active 8. (3 pts) How many stereoisomers are there of 2,3-dibromobutane? 4 sleeoisamvers (8 pts) Circle the letter of the statements that are true. a. Racemic mixtures are optically active Enantiomers have specific rotations that are equal, but have opposite signs 9. o adtc) Achiral molecules are optically inactive d Meso compounds contain equal amounts of enantiomers 4pts) Complete the Fischer...
Consider the following molecule, capsaicin, for the 13-15: HO Capsaicin 13. How many atoms are sp...
Consider the following molecule, capsaicin, for the 13-15: HO Capsaicin 13. How many atoms are sp hybridized in the above molecule? 14. How many sigma bonds are the Oxygens involved in? 15. What is the hybridization of the Nitrogen and it's shape (Hint: Go through CN and AXE notation)? 16. What is a possible a set of quantum numbers for a valence electron of Zirconium (Zr) 17. What is the electron configuration of Col?
For the molecule whose condensed structural formula is given below, decide if cis-trans isomers are possible....
For the molecule whose condensed structural formula is given below, decide if cis-trans isomers are possible. If they are, enter the name of the cis isomer in the first box and the name of the trans isomer in the second box. If cis-trans isomers are not possible, enter the name of the compound in the first box and leave the second box blank. Do not attempt to put cis or trans in italics. CH3CH2CH=CH2
Show how you would accomplish the following conversions a) trans-hex-3-ene to meso-hexane-3-4-diol. Please explain when to...
Show how you would accomplish the following conversions a)
trans-hex-3-ene to meso-hexane-3-4-diol. Please explain when to
rotate. Thank you !
Show how you would accomplish the following conversions. trans-hex-3-ene to meso-hexane-3,4-diol . ~ CH,C01H HO Chocolate HO rotate CH,CO,H HO HO HO OH Submit Request Answer Part D trans-hex-3-ene to (0,2)-hexane-3,4-diol ~ Ho t do anemie van OSO. rotate racemic (d.1) HO Но он ~ rotate CH CO, HO CHCOM enten met racemic (d.1) HOOH CHICOH HO racemic (d.1) Но...
The molecule below is: OH o OH Optically active Non superimposible on its mirror image Both...
The molecule below is: OH o OH Optically active Non superimposible on its mirror image Both (-) and (+) Achiral
4. Circle the molecule(s) that would be considered "optically active". но н CH3 навесно нн, сон...
4. Circle the molecule(s) that would be considered "optically active". но н CH3 навесно нн, сон CH2CHE
The molecule below is: ОН ОН Optically active Non superimposible on its mirror image Both (-) and (+) Achiral
20. Make a model of trans-1, 4-dimethylcyclohexane and cis-1, 4-dimethylcyclohexane. Draw their chair conformations below including the chair flip for each. Repeat questions 15-16 on this model Part III. Learning to Draw Molecules on a Computer Start the ACD ChemSketch programs and spend 15 minutes familiarizing yourself with their drawing capabilities. Practice using ChemSketch 2.0 to convert two dimensional structures to three dimensional structures and rotating and viewing three dimensional structures. 1. Based on the shape of the molecule, what...
please answer all
Question 1 2 pts Determine whether the molecule below is optically active. cannot determine O optically active O optically inactive Question 2 2 pts Determine the relationship between the two molecules below NH2 HO H3COOH identical enantiomers constitutional isomers diastereomers Question 3 2 pts Determine the relationship between the two molecules below H HOW enantiomers O identical constitutional isomers diastereomers D Question 4 2 pts Determine the total number of stereoisomers represented by the bond line drawing...
6 CHM 2440 (FA 2019) Sp hybridized atoms has a trigonal planar geometry of their hybridized orbitals. This will affect the geometry of the molecule- wben covalent bonds are formed, it makes the neighboring atoms coplanar. For example: CH,-CH, is a planar structure with both carbon and all four hydrogen atoms on the same plane. HiH Circle the carbon atoms that are co-planar in the structure below. (0.25 pt) CH3 H3C-CH2-C CH2-CH3 5. Give the IUPAC name for each of...
7. (9 pts) (Are the following optically active or meso? meso HyCHC OH HO opticaly actve active opti call active 8. (3 pts) How many stereoisomers are there of 2,3-dibromobutane? 4 sleeoisamvers (8 pts) Circle the letter of the statements that are true. a. Racemic mixtures are optically active Enantiomers have specific rotations that are equal, but have opposite signs 9. o adtc) Achiral molecules are optically inactive d Meso compounds contain equal amounts of enantiomers 4pts) Complete the Fischer...
Consider the following molecule, capsaicin, for the 13-15: HO Capsaicin 13. How many atoms are sp hybridized in the above molecule? 14. How many sigma bonds are the Oxygens involved in? 15. What is the hybridization of the Nitrogen and it's shape (Hint: Go through CN and AXE notation)? 16. What is a possible a set of quantum numbers for a valence electron of Zirconium (Zr) 17. What is the electron configuration of Col?
Show how you would accomplish the following conversions a)
trans-hex-3-ene to meso-hexane-3-4-diol. Please explain when to
rotate. Thank you !
Show how you would accomplish the following conversions. trans-hex-3-ene to meso-hexane-3,4-diol . ~ CH,C01H HO Chocolate HO rotate CH,CO,H HO HO HO OH Submit Request Answer Part D trans-hex-3-ene to (0,2)-hexane-3,4-diol ~ Ho t do anemie van OSO. rotate racemic (d.1) HO Но он ~ rotate CH CO, HO CHCOM enten met racemic (d.1) HOOH CHICOH HO racemic (d.1) Но...
The molecule below is: OH o OH Optically active Non superimposible on its mirror image Both (-) and (+) Achiral
4. Circle the molecule(s) that would be considered "optically active". но н CH3 навесно нн, сон CH2CHE
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