For the following structure, identify the spatial relationship between two or more hydrogens that are bonded to a single carbon atom. Highlight any homotopic hydrogens in red, enantiotopic hydrogens in green, and diastereotopic hydrogens in blue. H. H HH H D C
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- For the following structure, identify the spatial relationship between two or more hydrogens that are bonded to a single carbon atom. Highlight any homotopic hydrogens in red, enantiotopic hydrogens in green, and diastereotopic hydrogens in blue. CI H H HI C H C- -C. H H H —H H Ś 000 18 ArFor the following structure, identify the spatial relationship between two or more hydrogens that are bonded to a single carbon atom. Highlight any homotopic hydrogens in red, enantiotopic hydrogens in green, and diastereotopic hydrogens in blue. 00 HI H H H H H H H H X olo Ar 8. 囚For the following structure, identify the spatial relationship between two or more hydrogens that are bonded to a single carbon atom. Highlight any homotopic hydrogens in red, enantiotopic hydrogens in green, and diastereotopic hydrogens in blue. Try again HHH HH H Br
- The following model shows the 3D representation of methylcyclobutane. ball & stick v + labels - The molecular formula for methylcyclobutane is:Matching between the following pairs of structures and the sutible class? & NH H H H CH3 CH3 and CH3 Br Cl and and H H OH N CH3 CH3 H CH3 Br ClDraw all six ketone constitutional isomers of the formula C6H12O Follow the instructions and draw the five different possible arrangements of six carbon units. For parts A-C, draw only the six carbon atoms and Do Not draw the ketone. A:draw the structure containing six carbons in the longest parent chain. B: draw the two structures containing five carbons in the longest parent chain. C: Draw the two structures containing four carbons in the longest parent chain. D: Using the five structures from parts A,B,&C as a guide, draw the skeletal structures of the six constitutional isomers of C6H12O that are ketones.
- How could IR be used distinguish among these three compounds to O- H. O-H A ofExamine the ungraded ball-and-stick model to determine the three-dimensional structure of the molecule. On the corresponding 2D structure, draw one wedge bond and one dash bond over two existing bonds to indicate the same arrangement of atoms in space. The narrow part of each wedge-and-dash bond should be towards the same central carbon atom. Click on the three-dimensional molecular structure of (S)-1-chloro-2,3-dimethylbutane and drag to rotate it, or use the controls provided. 80 F3 $ 4 R F 000 COD F4 D V % 5 C T G MA F5 B OH 6 CL MacBook Pro Y Fo H & 7 N da F7 U * 00 8 M DII FO - Change two bonds to stereobonds. K Select Draw Rings More ////// 3 ( 9 H CH₂ */ CH₂ G DD F9 H O V H,C ) O command F10 P A C - H F11 Q2Q Cl { option + = F12 Erase = ] (1) deleHow many axial hydrogens are present?
- What is the condensed structural formula for the following molecule? H H C1H H-C- : Z―I OCH3NHCHCH2 OCH3NH(CHCH₂) (CH3)NHCHCH₂ C3H6N H C FC-HProvide The IL X H Convert Heic Similar Questi X diastereomers X C Which Of The x CQuestion 13 O X Provide The IU X Question 10 of 29 Provide the IUPAC name for the condensed structural formula shown here. CH3 CH3 CH3-C-CH2-CH-CH2-CH3 CH3 2,2-di meth yl-4-meth yl pent ane 2,2- 2,2,4- 3,5,5- | 2- 3- 4- tert- tetra di tri pent meth hept eth but hex ane yl ene MacBook Air 000 000 08 DDwhat is the BP range for hexane and toluene?