Write a molecular formula corresponding to the systematic n propane. Then provide a new main projection that illustrates the highest energy confirmation of n propane How long any C-C bond axis of the same.
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Q: В C
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Q: Select the correct Newman projection looking down the C2-C3 bond of the below structure. CI Н. H H3C…
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- Which of the following molecules is trans? CH, H,C H,C CH, CH, H,CMake a continuous model for C4H10 by using 4 black 4 hole carbon atoms, 10 white one hole hydrogen atoms, and 13 pink bonds. Then write in wedge dash notation C4H10 and add in missing hydrogen atoms.Place the following in order of decreasing dipole moment. |- CH4 II - CH3OH III - CH3SH III > | > || Il > | > II | > II| > | || > III > I | = II| > ||
- or each of the following molecules, construct the MOS from the 2p, atomic orbitals perpendicular to the plane of the carbon atoms. (a) Cyclobutadiene HC=CH НС—СН HC=CH НС —СH (b) Allyl radical H H H H C=C •C-C, H C-H H C-H H H Indicate which, if any, of these orbitals have identical ener- gies from symmetry considerations. Show the number of electrons occupying each w MO in the ground state, and indicate whether either or both of the molecules are para- magnetic. Assume that the C atoms in the allyl radical are all sp? hybridized. Activate io to SQ2. Draw a zig-zag representation for each molecule below showing all valence electrons on atoms other than carbon and hydrogen and include any formal charges should there be any (none of the compounds contain a ring of atoms).(a) CH3CH=CHCH(OH)CH3(b) (CH3)2CHCH2CO2CH2CH3Make three-dimensional drawings of the following molecules, and predict whether eachhas a dipole moment. If you expect a dipole moment, show its direction.(a) H2C꓿CH2(b) CHCl3(c) CH2Cl2(d) H2C꓿CCl2
- Isoniazid is used in the treatment of tuberculosis and multiple sclerosis. N I H Isoniazid A Lone pair A Lone pairs B Lone pair C Lone pair D Identify each lone pair as either localized or delocalized. Justify your answer in each case. B NH₂ NH₂ C D and is, therefore, and are, therefore, Vand is, therefore, and is, therefore,Curved arrows are used to illustrate the flow of electrons. Using the provided resonance structures, draw the curved electron-pushing arrows to show the interconversion between resonance hybrid contributors. Be sure to account for all bond- breaking and bond-making steps. Drawing Arrows :S: | :N:O KO ØThe bond angles marked a, b, and c in the molecule below are about :O: H :O: || | || -CC-O-H a b c H H O 109.5°, 120°, 109.5° 120°, 120°, 90° 120°, 120°, 109.5° O 109.5°, 90°, 120° and respectively. [CLO-1]
- Which is the correct newman projection for the following molecule (as drawn below assuming no rotation) when looking down the bond indicated by the arrow? 0 0 Me Me Et Me Me Et Me Me II….. H H H HConvert the following bond-line structure to a Newman projection (look from C5 to C4). Then draw the highest and lowest energy conformer for the molecule: H HClick on all of the atoms that make up the largest coplanar unit in the molecule below. H H H-C H H H-C-S H H