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- Draw a resonance structure, complete with all formal charges and lone (unshared) electron pairs, that shows the resonance interaction of the cyano with the ortho position in benzonitrile. CEN benzonitrile • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one.Draw 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.Choose the correct answer. Choose.. Choose... An alkyne with molecular formula C5H10 A ketone with molecular formula C4H8O A ketone with molecular formula C3H8O An alkene with molecular formula C5H8 An alkene with molecular formula C5H10 An aldehyde with molecular formula C2H40 An aldehyde with molecular formula CH4O H. A saturated hydrocarbon with molecular formula C6H14 Choose..
- Choose the correct answer. Choose.. Choose.. A saturated hydrocarbon with molecular formula C6H14 An alkyne with molecular formula C5H10 A ketone with molecular formula C4H80 An alkene with molecular formula C5H10 An aldehyde with molecular formula CH4O An alkene with molecular formula C5H8 A ketone with molecular formula C3H8O An aldehyde with molecular formula C2H4O Choose..7. Draw curved arrows indicating the movements of electrons between the following pair of resonance structures. Name the pattern of resonance shown. What is the hybridization of the carbon atoms? 8. Draw the remaining three resonance structures for the molecule in problem 7 above. 9. There are several possible forms of a trisubstituted cyclohexane with the formula C10H200. I have drawn four of them. From these, which one do you think is most commonly naturally occurring, and why? Which is least commonly occurring and why? HO HO" HO HODirection: Give what is being asked on the given organic compounds. Please be guided accordingly. NOTE: The highest score is 25 points, on the other hand, it is on the teachers' decision to give point if your answer is wrong to give way for considerations. CH₂ CH₂ CI I CH₂CH₂ NAME: CONDENSED FORMULA EXPANDED CONDENSED FORMULA: MOLECULAR FORMULA: C3 H7 b. NAME: CONDENSED FORMULA: EXPANDED CONDENSED FORMULA: MOLECULAR FORMULA: Br CHICHI CHO CH₂ CH₂
- For (A-G) fill in table with the missing information. Each molecule in each row should have a skeletal formula, an IUPAC name, and a functional class identified.What is the systematic name for the molecule depicted by the following bond line structure? Decide what the longest C-C chain is (parent) and then decide which substituents are there and how to number it to give the lowest locants. Make sure each substituent gets a locant. Separate letters from numbers by a dash, and numbers from each other by a comma. Do not put any spaces in your name.label alpha carbon, beta carbon, leaving group, primary secondary, tertiary, typea of functional groups Solve asap
- Write a molecule with a total of 16 carbons, with at least one aromatic group and one alkyl group in the structure for each of the organic compound classes given below. Name these molecules according to the IUPAC system. a) Write and name a heteroaromatic molecule. ( will have a total of 16 carbons) b) Write and name a benzaldehyde derivative. ( will have a total of 16 carbons) c) Write down and name a dithiol molecule. ( will have a total of 16 carbons)[Review Topics] Examine the geometry of the molecule in the 3D window. . Double-click on an atom, and then move cursor over another one to get a distance (click off of the molecule to end) Double-click on an atom, click on a second and move cursor over a third to get the angle about the second atom (click off of the molecule to end) Submit Answer Ⓒ Retry Entire Group JSmol The molecule has a carbonyl group. The molecule has one shorter carbon-to-oxygen bond distance and one longer one. A general functional group representation of the molecule i The substance is a(n) [References] 9 more group attemp RCHO RCOR* RCOOR RCOOH where R and R* are carbon groups. Previous Next Save anDetermine if each molecule below is an aldehyde, ketone or alcohol based on the ending. heptanal 3-methyl-2-pentanol 1. alcohol 3-methyl-2-pentanone 2. ketone cyclobutanone 3. aldehyde cyclopentanone 3-methyl-2-pentanal