Which reaction pathway is favored given the following substrate and conditions? ci NaBr Acetone O a....
What is the systematic IUPAC name for the following Organic compound? O a. Ethylpentanoate b. Pentylethanoate c. Octan-2,4-dione d. Butanoic methanoic anhydride e. 2,4-Dioxo)ethoxypentane f. Ethanoic pentanoic anhydride
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
Any help?! Which reaction pathway is favored given the following substrate and conditions? Ci xi NaBr Acetone a. SN2 b. Sni c. E1 d. SN2/E2 e. E2 f. Sn1/E1
Which reaction pathway is favored given the following substrate and conditions? ci NaBr Acetone a. E2 b. Syl El c SX2 d. SN 2 E2 e. E1 f. Sni
Which reaction pathway is favored given the following substrate and conditions? CH3OH -78 °C OTS a. Sn1/E1 b. Sn2/E2 CSN2 d. E1 e. E2 f. SN1
e reaction of (R)-2-bromopentane with an excess of sodium 51. Give the SN2product(s) for the reaction of (R)-2-bromopentane w methoxide. A) (S)-2-methoxypentane B) (R)-2-methoxypentane C) (S)-2-ethoxypentane D) (R)-2-ethoxypentane E) (R)-2-pentanol F) (S)-2-pentanol 52. What mechanism predominates in the reaction below? L CH.CH NaOCH, CH,OH A) SN2 B) SNl without rearrangement C) SNI with rearrangement D) E2 E) E1 53. Which of the following is the best method for preparing CH3Br? A) CH3OH + Br B) CH3OH + HBr C) CH3OH...
Question 7 [1.5 pts] Which one of the following statements about Reaction #6 is correct? Reaction #6 Н D CH2CI2 NaN3 E OThe major organic product arises from front face attack by the N3 anion at atom D O The major organic product arises from front face attack by the N3 anion at atom E OThe major organic product arises from back face attack by the N3 anion at atom D The major organic product arises from back face attack...
Which statement or set of conditions listed below is not consistent with an Syl reaction pathway? O a. Neutral nucleophile work just fine. b. The leaving group is typically the conjugate base of a strong acid. O c. The rate is not dependent upon the concentration of the nucleophile. d. The temperature is relatively "cooler" to reduce competing elimination products. e. The solvent is polar and aprotic. Of. The substrate has a leaving group that is typically on a 30,...