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A: The synthesis is as follows:
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Q: Which of the following compounds can exhibit cautomerism?
A: The compounds which differ only in the position of electrons and protons are termed as isomers.
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A: The line formula of oleic acid can be drawn as:
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A: The structure of pyruvic acid is
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Q: Classify attached transformation as an oxidation, reduction, or neither. (See attachment)
A:
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A: Define the term Calcination
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A: The anomer in which the alkoxy or hydroxyl group on the anomeric carbon is pointing downward is…
given all this information draw the strucutre.
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- Rank the following groups in order of decreasing priority. −H, −CH3, −Cl, −CH2ClHow many rings and π bonds are contained in compounds A—C? Draw one possible structure for each compound. a.Compound A has molecular formula C5H8 and is hydrogenated to a compound having molecular formula C5H10. b.Compound B has molecular formula C10H16 and is hydrogenated to a compound having molecular formula C10H18. c.Compound C has molecular formula C8H8 and is hydrogenated to a compound having molecular formula C8H16.How many rings and π bonds are contained in compounds A–C? Draw one possible structure for each compound. a. Compound A has molecular formula C5H18 and is hydrogenated to a compound having molecular formula C510H10. b. Compound B has molecular formula C10H16 and is hydrogenated to a compound having molecular formula C10H18. c. Compound C has molecular formula C8H8 and is hydrogenated to a compound having molecular formula C8H16.
- Answer the following questions about compound A, which contains a CH3 group and OH group bonded to the carbon skeleton that consists of three six-membered rings in the conformation shown a.) Are the CH3 and OH groups oriented cis or trans to each other?b.) Is a substituent on Ca that is cis to the CH3 group located in the axial or equatorial position? c.) Is an equatorial Br at Cb oriented cis or trans to the OH group?d.) Is the H atom on Cc located cis or trans to the OH group?e.) Is a substituent on Cd that is trans to the OH group located in the axial or equatorial position?Draw the three constitutional isomers having molecular formula C7H14 that contain a ve-membered ring and two methyl groups as substituents. For each constitutional isomer that can have cis and trans isomers, draw the two stereoisomers.Rank the following groups in order of decreasing priority. a.−F, −NH2, −CH3, −OH b.−CH3, −CH2CH3, −CH2CH2CH3, −(CH2)3CH3 c.−NH2, −CH2NH2, −CH3, −CH2NHCH3 d.−COOH, −CH2OH, −H, −CHO e.−Cl, −CH3, −SH, −OH f.−C≡CH, −CH(CH3)2, −CH2CH3, −CH=CH2
- Rings + Unsaturation --- Hydrogenation If compound A C51H81BrN5O3P3 is hydrogenated to give compound B C51H101BrN5O3P3. How many rings does compound A have? Assume that P has a valency of 5. Would the answer be 4 rings? Formula -> unsat + rings = 1+C +N/2 - H/2 - X/2Place the following compunds in order from lowest to highest boling points. Explain why you have ranked each compound C6H14 CH3OH H2O C3H8) How many stereogenic double bonds are in octa-1,3,5-triene? How many stereocentersare there?
- Neuroprotectin D1 (NPD1) is synthesized in the body from highly unsaturated essential fatty acids. NPD1 is a potent natural anti-inflammatory agent.a.Label each carbon–carbon double bond as conjugated or isolated. b.Label each double bond as E or Z. c.For each conjugated system, label the given conformation as s-cis or s-trans.Neuroprotectin D1 (NPD1) is synthesized in the body from highly unsaturated essential fatty acids. NPD1 is a potent natural anti-inflammatory agent. a.) Label each carbon–carbon double bond as conjugated or isolated.b.) Label each double bond as E or Z.c.) For each conjugated system, label the given conformation as s-cis or s-transRank the following groups in order of decreasing priority. a.−COOH, −H, −NH2, −OH b.−H, −CH3, −Cl, −CH2Cl c. −CH2CH3, −CH3, −H, −CH(CH3)2 d.−CH=CH2, −CH3, −C≡CH, −H