Treatment of 1-bromoheptane with excess sodium iodide in acetone gives as the major product: Select one:...
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
Homework Answers
Add Answer to:
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...
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...
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...
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...
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...
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...
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...
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...
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...
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.
(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
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
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
Most questions answered within 3 hours.
-
You capture data by having 8 people fill in 30 small dots on a
piece of...
asked 2 hours ago -
What are the z-values such that 70% of the area lies in the
middle of the...
asked 4 hours ago -
You borrow $29,500 to purchase a brand new car. The interest
rate is 6%, and the...
asked 4 hours ago -
The amount of time it takes an asteroid, whose average distance
from the Sun is 4.70...
asked 4 hours ago -
A 0.289 kg mass slides on a frictionless floor with a speed of
1.34 m/s. The...
asked 4 hours ago -
15.A box contains five red balls, three green balls, and two
yellow balls. Suppose you select...
asked 7 hours ago -
Assume you are given the following for Stackelberg industries:
Return on Assets (ROA) = 8%
Debt...
asked 6 hours ago -
an engineer proposes to use mmWave in 5G network to
increase data rate.
What are the...
asked 6 hours ago -
Explain the idea behind using SEMIJOIN in distributed
query processing.
asked 6 hours ago -
why
is context important in selecting and applying guidelines and
principles for interface design?
illustrate your...
asked 6 hours ago -
In a certain board game, a player rolls two fair six-sided dice
until the player rolls...
asked 7 hours ago -
You are going to deposit $3,200 in an account that pays .58
percent interest compounded quarterly....
asked 6 hours ago