Treatment of 1-bromoheptane with excess sodium iodide in acetone
gives
as the major product:
Select one:
a. 1-bromo-1,1-diiodoheptane
b. no reaction
c. 1-heptene
d. 1-iodoheptane
e. 1-bromo-2-iodo-heptane
Treatment of 1-bromoheptane with excess sodium iodide in acetone gives as the major product: Select one:...
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
Draw and name the SN2 major product formed when (2R,5S)-2-bromo-5-chlorohexane is treated with sodium iodide in acetone. (Use only one equivalent of NaI.)
Following are two diastereomers of 3-bromo-3, 4-dimethylhexane. On treatment with sodium ethoxide in ethanol, each gives 3, 4-dimethyl-3-hexene as the major product. One diastereomer gives the E alkene, and the other gives the Z alkene. Which diastereomer gives the E alkene? Following are two diastereomers of 3-bromo-2, 3, 4-trimethylhexane. On treatment with sodium ethoxide in ethanol, each gives 23, 4-trimethyl-3-hexene as the major product. One diastereomer gives the E alkene, and the other gives the Z alkene. Which diastereomer gives...
What is the major product resulting after heating 1-bromo-3-methylpentane with 2M sodium hydroxide: Select one: O a. 3-methylpent-2-ene b. 3-methylpent-1-ene C. 3-methylpentan-1-ol d. 3-methylpentan-2-01 o e. There is no reaction
Choose the reaction that is least likely to undergo an E2 reaction pathway. Question 2 NaOCH3 CH,он Br O он В кос(сH,) нос(CH,) Br D NaC CH CH2CN кос(CH) C НОС(CH,)з D O C O E Enter Your Answer: OA (R)-1-bromo-2-methylbutane undergoes substitution when reacted with sodium iodide (NaI) in acetone. Choose the major product obtained from this reaction. Question 3 A (R)-1-iodo-2-methyl butane B (S)-1-iodo-2-methylbutane C racemic 1-iodo-2- methylbutane D (R)-1-bromo-2-iodobutane E (S)-1-bromo-2-iodobutane F (S)-1-sodium-2-methylbutane A B F F...
1.1 What is the major product formed upon treatment of (R) 1-bromo-4-methylhexane with sodium cyanide? Draw the structure of your selection. a.(R) 1-cyano-4-methylhexane b.(S) 1-cyano-4-methylhexane c.(R) 4-methyl-1-hexene d.(S) 4-methyl-1-hexene 1.2 What is the major product formed upon treatment of (R) 2-bromohexane with sodium cyanide? Draw the structure of your selection a.(R) 2-cyanohexane b.(S)2-cyanohexane c. 1-hexene d. 2-hexene 1.3 Select the major organic product obtained from the following reaction 1.4 Select the major organic product obtained from the following reaction 1.5...
What is the major product resulting after heating 1-bromo-3-methylpentane with 2M sodium hydroxide What is the major product resulting after heating 1-bromo-3-methylpentane with 2M sodium hydroxide: Select one: a. 3-methylpent-2-ene O b. 3-methylpent-1-ene O C. 3-methylpentan-1-ol O d. 3-methylpentan-2-ol e. There is no reaction
19.54 predict the major product(s) from the treatment of acetone with the following: 19.54 Predict the major product(s) from the treatment of acetone with the following: (a) [H*1, NH3, (-H2O) (b) [H*], CH3NH2, (-H2O) (d) [H*], (CH3)2NH, (-H2O) (c) [H*], excess ETOH, (-H2O) (e) [H*], NH2NH2, (-H2O) (f) [H*1, NH2OH, (-H2O) (g) NaBH4, MeOH (h) RCO3H (i) HCN, KCN () EtMgBr followed by H2O (k) (C&Hs)3P=CHCH2CH3 (I) LIAIH4 followed by H2O
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...
(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