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A: Given reagent,
Q: Answer the question below directly. Why methanol is a good solvent for UV but not for IR?
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A: A question based on IR spectrum, which is to be accomplished.
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A: An azo coupling reaction involves reaction between a diazonium compound and any other aromatic…
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Q: hat's the azo-dye reaction test to this
A: To determine the azo-dye reaction test for the below reactant.
Q: hat is the purpose of adding CaCO3 or NaHCO3 in the Mohr Method determination of chloride? Than
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Q: Why methanol is a good solvent for UV but not for IR?
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Q: 7-9
A: TLC is an analytical technique which can be used to monitor the organic reaction transformations.…
Q: Question 10. Based on the electrostatic potential surface (EPS) maps of indole, benzene and pyridine…
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A: The structure of (2) is given to be:
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A: Infrared spectroscopy used in order to identify functional groups present in a compound
Q: the
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Q: 3. Give another dye that is made using diazonium salt chemistry/coupling reaction. Draw the dye as…
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Q: what are the IR spectra changes when monitoring the following reaction?
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A: A question based on IR spectra, which is to be accomplished.
Q: Write down the reaction and mechanism for the experiment.
A: Reaction and mechanism given below.
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Q: 3. Give another dye that is made using diazonium salt chemistry/coupling reaction. Draw the dye as…
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Briefly explain based on the IR spectra how well the reaction worked.
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- CH-(CH₂)-CH-CH₂-CH₂-COOH 1 CH3-CH-CH-CH3 in the presence of LiAIH4 as catalyst; is obtained: oy) 4-secbutyl decanoic acid np) 4-secbutyl-2-decanol kv) Secbutyl decanoate di) 4-secbutyl decanal By reducing the compoundWhat is the major organic product obtained from the following reaction? H₂Cr₂O7 H₂SO4, H₂O OH A) 1-butene, CH3CH2CH-CH₂ B) butanal, CH3CH₂CH₂CHO C) butanone, CH3CH₂COCH3 D) butanoic acid, CH3CH2₂CH₂COOHCyclohexanone can be effectively oxidized to adipic acid by treatment with which two of the following compounds? O KMNO4 or HNO3 O HOCI or HNO3 O PCC or Na;Cry03 O LIAIH or NaBH4 O None of these choices
- Acid-Catalyzed Nucleophilic Addition - Addition of Amines: Imine and Enamine Formation (mechanism!) 1° amines add to form imines (C=NR), and 2° amines yield enamines (R₂N-C=C) CH,CH,NH2 H30* + H* - H₂O - Alcohols Addition to yield hemiacetals (hemiketals), acetals (ketals) -C(OR')2 (mechanism!) H30Ⓡ + N-H CH3CH₂OH (2 equiv.)An acetal produces the following three compounds upon hydrolysis. Of acetals A-E which could it be? H3CO OCH3 П A B U D Acetal A H2O H₂SO4(cat.) замен поста "OCH3 В + HO. H₂CO ОН D + OCH3 CH3OH E OCH3 "OCH3OH h) Draw a stepwise mechanism for the following reaction. NH2OH MEOH %3D i) Suggest two methods to synthesize the alkene below from cyclopentanone.
- Propose a synthesis of the topical anesthetic cyclomethycaine from 4-hydroxybenzoic acid, 2-methylpiperidine, and any other necessary reagents. HN' + HO. НО Cyclomethycaine 4-Hydroxybenzoic acid 2-MethylpiperidineMy C mentProblemID=192850292 A&P II Mast o ethyl butanoate ▼ PSY Connect Part A Pears Bb 1574 b Ansv G great H₂C NN Course Home pt My [ chem in career H 12D EXP CONT Predict the major organic product formed when the compound shown below undergoes a reaction with LiAlH4. Interactive 3D display mode CH3 Chen Chen Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Ter * I ο phys G phys N OProvide reagents and conditions to produce the products indicated. EtO COET HO 요 요 OEt + EtO COET (2.0 equiv)
- Are the following reactions stere oselecth ve? (R)-2- bromo pen tune reacts with CH3OH atroom tem perature ?) 2) (BR)3-bromo3,4-dimetny Ihexane is refluxed with KOH 3) (R)-3-iodohexane is refluxed with Hz 0 A) (S)4-iodononane is refluxed with KNgWhich of the following will be the dominant product of the dehydration reaction shown? H;PO, H2O. A но (A) (B) (C) (D) Compound B Compound C OCompoundD OCompound A nintc)Devise a synthesis of (E)-tetradec-11-enal, a sex pheromone of thespruce budworm, a pest that destroys fir and spruce forests, fromacetylene, Br(CH2)10OH, and any needed organic compounds orinorganic reagents.