Select the correct common name and/or IUPAC name for the structure: Which name(s) fit this structure? 1-methylpropanone 2-butanone or butan-2-one butanal 3-butanone or butan-3-one
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A: Select the correct IUPAC name for:
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Q: 8. 4-Methylbutanal 9. 2,2-Dimethyl-3-butanone 10. 2-Pentanal
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A: The given compounds is : The proper structure with carbon and hydrogen atoms can be drawn as :
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Q: Draw an appropriate structure for each of the follow 2-Hydroxy-4'-nitrobenzophenone
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- Draw the structures based on iupac name digitally (highly suggest chem-space .com for easy drawing) 1,1-Dibromo-4-isopropylcyclohexane 4-sec-Butyl-2-chlorononane 1.1-Dibromo-4-Pert-Butylcyclohexane(a) One test for the presence of an alkene is to add a smallamount of bromine, which is a red-brown liquid, and lookfor the disappearance of the red-brown color. This test doesnot work for detecting the presence of an aromatic hydrocarbon.Explain. (b) Write a series of reactions leading topara-bromoethylbenzene, beginning with benzene andusing other reagents as needed. What isomeric side productsmight also be formed?Explain briefly and clearly the following concepts, taking as reference the molecule of n-butane and the corresponding drawings or illustrations. See pages 149-152 of the book Organic Chemistry, sixth edition (J. G. Smith). 4. What is steric hindrance in a conformation? Then draw a picture to illustrate the concept? 5. What is the torsional stress of a conformation? Then draw a picture to illustrate the concept? 6. Describe 1,3-diaxial interaction and illustrate with a specific example.
- Referring to the named structures below, Choose:A if 1 st statement is true and the second statement is falseB if 1 st statement is false and the second statement is trueC if both statements are trueD if both statements are false 1. I: Structure A is an aromatic compoundII: Structue B is an alkane2. I: Structure C is not an aromatic compoundII: Strucure C and D are aliphatic hydrocarbon3. I: Structure F is not an aromatic hydrocarbonII: Only F is hydrocarbon4. I: Only Structure G will decolorize bromine solutionII: Structure H will produce brown solution upon basic oxidation5. I: Structure J will produce brown precipitate when potassium permanganate was addedII: Structure I will broduce yellow oil upon nitration6. I: Compound K is an aldehydeII: Compound L is an ketone7. I: Structure M is not an aldehydeII: Structure N is a ketone8. I: DNPH test cannot differentiate O and PII: Lucas test can differentiate O and P9. I: Compound Q will not react in Lucas testII: Compound R will react…Provide a molecule that contains the indicated functional groups and molecules. Each functional group must be single on your examples. Give an IUPAC accepted name for your molecules. a) Bicyclo compound: Alcohol (alcohol functional group must be on the 3° carbon atom), alkene, one cyclohexane and one cyclopentane. Plz do Asap ...! And send ur ans in clear manner ...!Draw all possible constitutional isomers for C2H6O and give common and IUPAC names for each structure.
- it's organic chemistry btw!Provide the E2 mechanism for β-elimination reactionemploying 2-chloro-2-methylbutane to prepare 2-methyl-2-butene and 2-methyl-1-butene reaction. Use the actual structures of thereactants and products. Explain which of the alkenes is the major product ofthis reaction ?Write a complete chemical equation showing reactants, products, and catalysts needed(if any) for the following reaction and (2) Draw and name the organic compound found inevery reaction.(Use condensed structural formula) (A) Reaction of cis-3,3-Dimethyl-4-propylocta-1,5-diene with two mole of HBr(B) Reaction of trans-1-Bromo-3-chlorocyclopentane with potassium hydroxide(C) Formation of Gilman reagent using isopropyl bromide
- When two six-membered rings share a C—C bond, this bicyclic system is called a decalin. There are two possible arrangements: trans-decalin having two hydrogen atoms at the ring fusion on opposite sides of the rings, and cis-decalin having the two hydrogens at the ring fusion on thesame side.a.Draw trans- and cis-decalin using the chair form for the cyclohexane rings. b.The trans isomer is more stable. Explain why.Compound A is branched and optically active and con-tains C, H, and O. (a) A 0.500-g sample burns in excess O₂ toyield 1.25 g of CO₂ and 0.613 g of H₂O. Determine the empiricalformula. (b) When 0.225 g of compound A vaporizes at 755 torrand 97C, the vapor occupies 78.0 mL. Determine the molecularformula. (c) Careful oxidation of the compound yields a ketone.Name and draw compound A, and circle the chiral centerDraw and name all of the structural isomers possiblefor an alkyl halide with no branches and the molecularformula C 5 H 10 B r 2