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Name the following molecule. Include all stereochemical assignments in your name.
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- 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.Draw a resonance structure, complete with all formal charges and lone (unshared) electron pairs, that shows the resonance interaction of the chloro with the para position in chlorobenzene. 0 chlorobenzene • 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. . 99-85 On [F ChemDoodleⓇI need to know the names of these two structurers for my notes but I am not sure how to name them.
- Question 15 In the blank for each molecule, enter A, B or C according to the code below: A-aromatic if planar B anti-aromatic if planar C-non-aromatic (does not matter if it is planar or not because other conditions for aromaticity or anti- aromaticity are not met) For those with more than one ring, consider the molecule as a WHOLE, rather than as separate rings. So if all of the rings together don't make for an aromatic molecule, then choose B or C. NH₂ 0₂ blank 1 blank 8 blank 2 blank 9 blank 3 s-cis blank 10 blank 11 N: blank 4 blank 12 blank 5 blank 13 blank 6 blank 14 Å blank 7 Q..z-z Ⓒ.H N-HPlease help , will provide helpful ratings for solving all 4 subparts only. Draw the skeletal structures that correspond to the following systematic (IUPAC) names.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.
- Name the following unbranched molecules from the numbered cards. When using a locator number use a dash to separate the number from the name. Type all answers in lowercase letters only. Name cards: 3,4,7,8,12,13,16,18,19,20,21,26Create Newman projections depicting conformations along the carbon-carbon bond described above in the lowest energy staggered conformation, gauche conformation, and highest energy eclipsed conformation. Appropriately label these conformations Please draw each out separately and do not just draw arrows on the molecule. OH HO HO. ОН ОНDirection: 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
- Name according IUPAC rule, the following molecule (with configurations if needed). You will give the name as the following, X for the positions and no space between characters : (XE,XR,XS)-X-methyl... Он NH, ОН6. Use the molecule below to answer the following questions. a) Name the following molecule. b) Why is it necessary to provide R or S designation in order to clearly communicate molecular structure for this molecule? c) How many stereoisomers of this molecule are possible? Which of them are enantiomers to each other? Which are diastereomers? SH ICNPlease help with all of the blank options. Draw ALL LONE PAIRS. Ignore stereochemistry.