What is the IUPAC name of the aldehyde or ketone starting material needed to make each of the following compounds using an oxidation or reduction reaction? (а) СНз—ОН CH3 CH3 (b) CH3-CH-CH–OH (c) CH3-C-OH
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- 12 Write the IUPAC names for these compounds. O (a) CHO CHOH (c) | CHOH I CH₂OH OH (b) (d) CHO NH₂ OCH₂-CH₂-CH₂-C-OH butanoic acid CH₂ HO–C–CH,CHCH,—CHO 3-methylpentanoic acid Name each carboxylic acid. (a) HO CH₂ CH₂ 99 - 0 B) CHICHICIO CH, Draw a condensed structural diagram for each carboxylic acid (a) Hexanoic acid (b) 3-propyloctanoic acid IWhat is the IUPAC name for the following compound? CH₂CH₂OH CH3CH₂C=CCH₂CH3 CH3 (A) 3-methyl-4-ethyl-3-hexen-6-ol B 4-ethyl-3-methyl-3,6-hexenol 3-ethyl-4-methyl-3-hexen-1-ol 3-methyl-4-(2-hydroxyethyl)-3-hexene E 3-(2-hydroxyethyl)-3-methyl-3-hexene
- Name the following ketones and aldehydes. When possible, give both a common name and an IUPAC name.(a) CH3CO(CH2)4CH3Draw a structural formula for the product formed by treating each compound with warm chromic acid, H2CrO4:(a) CH3(CH2)4CH2OH (b) (Picture attached) Please name both of the products, thanks!Give a systematic (IUPAC) name for each diol.(a) CH3CH(OH)(CH2)4CH(OH)C(CH3)3 (b) HO¬(CH2)8¬OH
- What product forms when the compound below is treated with Benedict's reagent? CHO H -C-OH CH,OH A) ÇH,OH H –Ç–OH CH,OH B) СНО C=0 CH,OH C) ÇOOH Н—С—ОН CH,OH D) ÇH,OH Но—ҫ—ОН CH,OH MacBook Air3) Which aa has the strongest acid side chain? a) b) H2N -CH-ö OH H,N -CH-C- OH CH2 ČH2 CH2 CH2 OH NH2 c) d) H2N -CH-ö OH H2N- CH OH CH2 CH-OH ČH3 OH 4) In order to oxidize an alcohol to aldehyde we use А) РСС В) НCL С) НЗО+Provide the major organic product of the following reaction. but-1-yne 1) Sia₂BH 2) H₂O₂, OH What is it called when an enol converts to a keto? A) Keto-enol isomerism B) Keto-enol tater tot-ism C) Keto-enol conversion D) Keto-enol tautomerism
- c) rite in the reagent(s) over the arrow. a) C6H5N₂+ b) C6H5C=N H3C- An OH H₂C → benzene H3C benzylamine CI CH3Pick the best IUPAC name for the following molecule: H3C-O CH3 CH3 H3C- O 2,4,5-trimethylheptanal O5-methoxy-2,4-dimethylheptanoic Acid O 5-methoxy-2,4-dimethylheptanal 5-methoxy-2,4-dimethylheptan-1-olGive a systematic (IUPAC) name for each diol.(a) CH3CH(OH)(CH2)4CH(OH)C(CH3)3