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- Draw the 4 skeletal structures of all isomers of C₆H₁₂ that have the (E)-configuration.How many [A] dand [B] T bonds are in the H2C=C=CH2 molecule?DHA is a fatty acid derived from fish oil and an abundant fatty acid in vertebrate brains. Hydrogenation of DHA forms docosanoic acid [CH3(CH2)20CO2H], and ozonolysis forms CH3CH2CHO, CH2(CHO)2 (five equivalents), and HCOCH2CH2CO2H. What is the structure of DHA if all double bonds have the Z configuration?
- For which of the following molecules are there two unique configurations about the double bond? Explain. (a) (CH3)2C=CHCI; (b) H2C=CHCH,CH3; (c) CIHC=CHBr; (d) HC=CCH=CHCISelect the bonds in the 3D representation of methyl urethane below that are multiple bonds. (Hint: Consider the number of bonds attached to an atom in the image compared to the normal valence of that atom. In a valid structure, the number of bonds to an atom will equal the valence of that atom.) • Gray = C: white = H; red = 0; blue = N; dark green = Cl; brown = Br; light green = F; purple = 1; yellow = S: orange = P. • Double click to select bonds. You can zoom in and out using the mouse scroll wheel (or pinch to zoom on touch screens). ●The pentadienyl radical, H2C“CH¬CH“CH¬CH2#, has its unpaired electron delocalized over three carbon atoms.(a) Use resonance forms to show which three carbon atoms bear the unpaired electron.(b) How many MOs are there in the molecular orbital picture of the pentadienyl radical?
- Your chemistry professor draws a number of molecules on the board: (1) CH4 ; (2) H2C=CH2 ; (3) H2C=C=CH2 ; and (4) H2C=C=C=CH2. You muse about all the molecules that chemists draw on a two-dimensional board and wonder which ones are actually planar, existing basically as they appear on the board, and which ones are not plane but rather three-dimensional. Answer ALL of the following questions. What are the specific orbital overlaps (i.e., sp3-sp3) that are in each of the molecules? What are the bond angles for each central atom in each molecule? Which molecules are planar and which are non-planar?Your chemistry professor draws a number of molecules on the board: (1) CH4 ; (2) H2C=CH2 ; (3) H2C=C=CH2 ; and (4) H2C=C=C=CH2. You muse about all the molecules that chemists draw on a two-dimensional board and wonder which ones are actually planar, existing basically as they appear on the board, and which ones are not plane but rather three-dimensional. Answer the following questions. What is the geometry and hybridization of the carbon in CH4? What is the geometry and hybridization of each central carbon atom in the remaining molecules? Draw each molecule showing the bonds and identify each bond in all the molecules as s or p. What are the specific orbital overlaps (i.e., sp3-sp3) that are in each of the molecules? What are the bond angles for each central atom in each molecule? Which molecules are planar and which are non-planar?ch 7 1: photosynthesis uses 690-nm light to convert CO2 and H2O into glucose and O2. claculate the frequncy of this light.
- Draw the line-bond structure of oleic acid (cis-9-octadecenoic acid), CH3(CH2)7CH=CH(CH2)7COOH, at physiological pH. You do not need to draw hydrogen atoms attached to carbon atoms.When B-carotene is oxidised in vivo, it breaks in half and forms two molecules of retinal (vitamin A), which is a precursor to the pigment in the retina responsible for vision. The conjugated system of retinal consists of eleven C atoms and one O atom; see the structure of the molecule here: H3C CH3 ÇH3 ÇH3 `CH3 In the ground state of retinal, each level up to n = 6 is occupied by two electrons. Assuming an average inter-nuclear distance of 140 pm, use the particle-in-a-box model to calculate: a. the separation in energy between the ground state and first excited state in which one electron occupies the state with n = 7, and b. the frequency of the radiation required to produce a transition between these two states.Predict the H¬C¬H and C¬C¬C bond angles inpropyne: