(S)-3-chloro-3-methylhexane is reacted with sodium iodide in water Select all products that are formed.
(R)-2-iodo-3-methylhexane | ||
(S)-3-iodo-3-methylhexane | ||
(R)-3-iodo-3-methylhexane | ||
(E)-3-methylhext-3-ene | ||
(Z)-3-methylhext-3-ene | ||
(S)-2-iodo-3-methylhexane |
Answer. (S)-3- chloro-3- methyl hexane is reacted with NaCl and H2O produce (S)- 3-iodo-3-methylhexane and (R)-3-iodo-3-methylhexane.
Because rxn follow SN1 mechanism and form carbonation, carbocation is planer intermediate thus attack of Iodine ion attack from left and right,gives 2 product.
(S)-3-chloro-3-methylhexane is reacted with sodium iodide in water Select all products that are formed.
R)-2-iodo-3-methylbutane is treated with sodium hydroxide. Select all products that are formed.2-methylbutan-1-ol3-methylbut-1-ene(S)-3-methyl-2-butanol(R)-3-methyl-2-butanol2-methylbut-2-ene2-methylbutan-2-ol
(R)-2-iodo-3-methylbutane is treated with sodium bromide in acetone. Select all products that are formed.2-methylbut-2-ene(R)-3-methyl-2-butanol(S)-2-bromo-3-methylbutane3-methylbut-1-ene2-methylbutan-1-ol2-methylbutan-2-ol
Give the name of the product formed when 1-chloro-4-methylpentane is reacted with sodium iodide in acetone. T T T Arial 3 (12pt)
S-3-chloro-3-methylhexane reacts with an iodide anion, I-. a) Will this reaction proceed via an SN1, SN2, E1, or E2 reaction mechanism? b) What is the IUPAC name of the product(s) of this reaction? Include R and S designations if relevant. c) After the reaction has occurred, will the product solution be optically active?
1.1What is the major product formed upon radical bromination of (S)-3-methylhexane? Select the best response. Draw the full mechanism. A. (S)-3-bromo-3-methylhexane B. (R)-3-bromo-3-methylhexane C. A mixture of (R) and (S) 3-Bromo-3-methylhexane D. (3R)-1-bromo-3-methylhexane 1.2 What is the major product obtained from the reaction of 2-methyl-2-butene with hydrogen bromide in the presence of peroxides?Select the best response. Draw the mechanism. A. 2,3-dibromo-2-methylbutane B. 2-bromo-3-methylbutane C. 2-bromo-2-methylbutane D. (E)-1-bromo-2-methyl-2-butene 1.3 There are 4 major products formed upon treatment of (E)-3-methyl-2-hexene with HBr...
on (R)-1-bromo-2-methylbutane undergoes substitution when reacted with sodium iodide (Nal) in acetone. Choose the major product obtained from this reaction. A (R)-1-iodo-2-methylbutane B (S)-1-iodo-2-methylbutane C racemic 1-iodo-2-methylbuta D (R)-1-bromo-2-iodobutane E (S)-1-bromo-2-iodobutane F (S)-1-sodium-2-methylbutane Enter Your Answer: OA OB OC OD OE OF B Incorrect
(R)-3,3-dimethylpentan-2-ol is heated with concentrated sulfuric acid Select all products that are formed.2,3-dimethylpent-2-ene(Z)-3,4-dimethylpent-2-ene3,3-dimethylpent-1-ene(E)-3,4-dimethylpent-2-ene3,3-dimethyl-pent-2-ene(S)-3,3-dimethylbutane-2-thiol
2-chloro-2-methylhexane is reacted with methanol. What is the IUPAC name of the single major expected E1 product of this reaction? Do NOT include stereochemistry (E/Z) in the name. The name must be correctly spelled and properly formatted (e.g. dashes, spaces, numbers, etc) according to IUPAC rules for credit.
Which of the following would be the substitution product or products if ( R)-3-chloro-3-methylhexane were allowed to react with methanol? Mark all that apply
(R)–3-chloro-2-methylhexane may undergo a nucleophilic substitution reaction in the presence of sodium ethoxide and ethanol. Complete the mechanism and draw the products of the reaction. <Chapter 7 SN2 and E2 Reactions of Alkyl Halides DOCH: FU MacBook Air