Q)1) The correct answer is option-B.
The IUPAC Name of the given compound is- 2-Ethyl-7-oxodecanoic acid.
Q)2) The correct answer is option-C.
The mechanism proceed in low concentration of nucleophilic/base in polar protic solvent is - Sn1, E1.......
help pleaseee What is the systematic IUPAC name for the following Organic compound? OH a. 2-Ethyl-1,7-dioxodecan-1-ol...
What is the systematic IUPAC name for the following Organic compound? OH O a. 2-Ethyl-7-oxodecanoic acid O b. 2-Ethyl-1,7-dioxodecan-1-ol c. 3-Carboxy-8-oxoundecane d. 9-Ethyl-4-oxodecanoic acid e. 1-Hydroxydecan-1,7-dione f. 9-Ethyl-4-oxodecanal What is the correct IUPAC name for the following alkene? CH3 CH3CH2CHC=CH2 CH2CH3 a. 2-(sec-butyl)but-1-ene b. 3-isobutylbut-3-ene c. 4-ethyl-3-methylpent-4-ene d. 2-ethyl-3-methylpent-l-ene e. 3-methyl-4-ethylpent-4-ene f. 2-ethyl-3-methylhex-2-ene g. octene
What is the systematic IUPAC name for the following Organic compound? ОН O o a. 3-Carboxy-8-oxoundecane b. 1-Hydroxydecan-1,7-dione c. 9-Ethyl-4-oxodecanoic acid d. 2-Ethyl-1,7-dioxodecan-1-01 o e. 9-Ethyl-4-oxodecanal f. 2-Ethyl-7-oxodecanoic acid
Which mechanism(s) listed below generally proceed(s) smoothly when a low concentration of neutral nucleophile base is used in the presence of a polar protic solvent? O a. Sy2 b. Syl and El c. El d. E2 e. Si f. Sn2 and E2
What is the systematic IUPAC name for the following Organic compound? -CEN a. 3-Phenylpropanenitrile b. 1-Cyano-2-phenylethane c. 2-Cyano-1-Phenylethane d. Cyclohexatrienylethanenitrile e. Benzonitrile f. 2-Phenylethanenitrile What is the systematic IUPAC name for the following Organic compound? o a. Pentanoic propanoic anhydride b. Pentylbutanoate c. Propylpentanoate d. Decan-4-one. e. Butylpentanoate f. Pentoxybutyl ketone What is the systematic IUPAC name for the following Organic compound? o a. Butanoic methanoic anhydride b. Ethanoic pentanoic anhydride c. Octan-2,4-dione O d. Pentylethanoate e. Ethylpentanoate f. 2,4-(Dioxo)ethoxypentane
What is the IUPAC name of the given molecule? OH Br 1-bromo-2-ethyl-2-hydroxy-3-methylpentanoic acid 2-ethyl-3-methylpentan-2-ol-1-carboxyl bromide 2-ethyl-3-methyl-2-ol-pentanoyl bromide O2-ethyl-2-hydroxy-3-methylpentanoyl bromide What statement is TRUE about the mechanism for the reaction shown here? CH,(CH)2CO,CH, NaOH CH3(CH12COCH excess heat CH3(CH)2CO,CH2 Water attacks the carbonyl carbon to form a tetrahedral intermediate. The first step of the reaction involves protonation of the ester carbonyl oxygen. One of the products formed is glycerol. The hydroxide deprotonates the alpha carbon. Which bases among the following is/are used...
[Review Topics) (References) Give an IUPAC name for the compound below. Accepted names for branched alkyl groups are isopropyl, isobutyl, sec-butyl, and tert-butyl. CH2CH3 CH3CH2CH2CCH2CH3 Submit Answer Retry Entire Group 9 more group attempts remaining The two reactants shown below are combined to bring about a nucleophilic substitution reaction. Br NaOCCH, . CH3CH2CHCH 1. none h. HBr 1.H20 e. "CCH3 f. Br j. Nat 9. HOCCH3 k. "OCCH3 Which letter designates the electrophilic carbon at which substitution occurs? (If no...
OH 8. What is the correct IUPAC name of the following compound? A) (4R)-4-hydroxymethyl)-4-isobutyl-2-vinylheptane B) (2R)-2-isobutyl-4-methyl-2-propyl-4-penten-1-ol (48)-4-hydroxymethyl)-6-methyl-4-propyl-2-vinylheptane D) (28)-2-isobutyl-4-methyl-2-propyl-4-penten-1-ol E) (4R) 4(hydroxymethyl)-6-methyl-4-propyl-2-vinylheptane F) (48)-4-(hydroxymethyl)-4-isobutyl-2-vinylheptane