(R)-3,3-diethylcyclohexanol Potassium tert-butoxide ←→ O Ask Copilot 15. Which of the following can react as a nucleophile? (A) (CH3)3B (B) (CH3)3CH C(CH3)3N (D) (CH3)30* (A) ме Mc -B- -

Arrange the following compounds in decreasing order of acidity * |- CICH2CH2CH2COOH Il - CH3CH2CHCICOOH III – CH3CHCICH2COOH III > I> || O I > II > || O I > I| > II III > || >|

(a) Draw the products (including stereoisomers) formed when 2methylhex-2-ene is treated with HBr in the presence of peroxides. (b) Draw the products (including stereoisomers) formed when (S)-2,4dimethylhex-2-ene is treated with HBr and peroxides under similar conditions.

Draw the line structure of the following compound. (2E,5R,7Z)-3-benzyl-8-bromo-4-(1-chloroethyl)-N-ethyl-7-methoxy-N,9-dimethyl-2,7-decadien-5-amine

Draw the formulas of the reactants and products of the reaction: 2-ethylbutanoyl bromide with excess ethylmagnesium bromide and heating the product with concentrated H2SO4.

Draw the product formed when CH3CH2C=CH is treated with each of the following sets of reagents: (a) H2O, H2SO4, HgSO4; and (b) R2BH, followed by H2O2, HO−.

(R)-2-bromobutane + CH3OH →

Draw the organic products formed when cyclopentene is treated withfollowing reagent.  [1] CH3CO3H; [2] H2O, HO−

What functional group is shown here: CH3CH₂COOH carboxylic acid ether alcohol ketone aldehyde

draw the structure for this compound