This question deals with epoxide formation. (a) Draw the skeletal structure of(Z)-3-methyl-2-pentene (b) Draw the skeletal...
(a) Draw the skeletal structure of(Z)-3-methyl-2-pentene
(b) Draw the skeletal structure of one of the enantiomers (thatmeans you have to show wedge/dash bond(s)) formed when(Z)-3-methyl-2-pentene reacts with Br2 in the presence of water.
(c) Draw the skeletal structure of the epoxide formed from yourproduct from (b) when it reacts with sodium hydroxide (you need toshow wedge/dash bond(s)).
(d) Draw the skeletal structure of the major organic product from(c) when it reacts with sodium methoxide in methanol-water solventfollowed by an acid workup. (Experimental data: the eliminationproduct is not the major organicproduct.)
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This question deals with epoxide formation.
(a) Draw the skeletal structure
of(Z)-3-methyl-2-pentene
(b) Draw the skeletal...
Draw the major product formed when the following epoxide reacts with methanol in the presence of sulfuric acid. Use w...
Draw the major product formed when the following epoxide reacts
with methanol in the presence of sulfuric acid. Use wedge/dash
bonds, including H\'s at each stereogenic center, to show the
stereochemistry of the product.
Draw the major product formed when the following epoxide reacts with methanol in the presence of sulfuric acid. Use wedge/dash bonds, including H\'s at each stereogenic center, to show the stereochemistry of the product.
Draw the major product formed when the following epoxide reacts with methanol in the presence of sulfuric acid. Use wedge/dash bonds, including H\'s at each stereogenic center, to show the stereochemistry of the product.
References) Draw the structure of the bromohydrin formed when (E)-3-methyl-3-hexene reacts with Br2/H20. Use the we...
References) Draw the structure of the bromohydrin formed when (E)-3-methyl-3-hexene reacts with Br2/H20. Use the wedge/hash bond tools to indicate stereochemistry where it exists. If the reaction produces a racemic mixture, draw both stereoisomers. Separate multiple products using the + sign from the drop-down menu. е CH3 H,с Br CHy ChemDoodle ChemDoodle"
Draw the skeletal structure of the major organic product of (3S,5S)-5-chloro-2,3-dimethyloctane when it reacts with sodium...
Draw the skeletal structure of the major organic product of (3S,5S)-5-chloro-2,3-dimethyloctane when it reacts with sodium iodide in acetone. please use stick and wedge bonds
1. Draw a structure for: (Z)-3-Bromo-2-hexene (Z)-1-methylcyclononene (3Z,6E)-1,3,6-Octatriene (E)-2-methoxy-2-pentene (3S,4S)-4-methyl-3-hexanol (1R, 3S)-3-methylcyclohexanol
1. Draw a structure for: (Z)-3-Bromo-2-hexene (Z)-1-methylcyclononene (3Z,6E)-1,3,6-Octatriene (E)-2-methoxy-2-pentene (3S,4S)-4-methyl-3-hexanol (1R, 3S)-3-methylcyclohexanol
The tosylate of (2R, 3R)-3-phenylbutan-2-ol undergoes an E2 elimination on treatment with sodium ethoxide. Draw the...
The tosylate of (2R, 3R)-3-phenylbutan-2-ol undergoes an E2 elimination on treatment with sodium ethoxide. Draw the structure of the alkene that is produced. Use the wedge hash bond tools to indicate stereochemistry. You do not have to explicitly draw H atoms. If a group is achiral, do not me wedged or hashed bonds on it. Predict the major alkene product of the following E1 reaction: Amines are converted into alkene5, by a two-step process called the Hofmann elimination. S_N 2...
6) Draw the structure of (Z)-1-chloro-2-methyl-2-butene. 7) Draw the curved arrows to show how CH3CH=CHCH2CH3 reacts...
6) Draw the structure of (Z)-1-chloro-2-methyl-2-butene. 7) Draw the curved arrows to show how CH3CH=CHCH2CH3 reacts with HBr to form a carbocation first, and then forms 2-bromopentane. (this is 2 steps) 7) 8) 8) Predict the product(s) of the following reaction based on the curved arrows: Make sure to include + and- charges where appropriate. -C-NH2 CH CHy HO 9) Based on the following reaction coordinate diagram: Which compound, A or C, is formed faster from B? Which is more...
Draw the structure(s) of the major organic product(s) of the following reaction, omitting the phosphine oxide....
Draw the structure(s) of the major organic product(s) of the following reaction, omitting the phosphine oxide. + 2 H2C=PPhg H H • You do not have to consider stereochemistry • li no reaction occurs, draw the organic starting material. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner • Separate multiple products using the + sign from the drop-down menu. P wat opy A (C4H100) reacts with phosphorus tribromide to give...
Which of the following correctly reflects relative stabilities of carbocations? 3 degree allylic > 2 degree...
Which of the following correctly reflects relative stabilities of carbocations? 3 degree allylic > 2 degree > 1 degree benzylic methyl > 2 degree benzylic > 3 degree 3 degree benzylic > vinyl >1 degree 2 degree allylic > 2 degree > vinyl 1 degree benzylic > 3 degree > 3 degree allylic Dehydrohalogenation of 2-bromobutane in the presence of a strong base proceeds via which of the following mechanistic pathways? S_N1 S_N2 E1 E2 none of the above Which...
please help me with questions from 3-10! and the bonus. thank you so much Directions: Place...
please help me with questions from 3-10! and the bonus.
thank you so much
Directions: Place your answers to the following questions in the provided spaces. (12 PTS) 1. What is the hybridization of the carbon atoms numbered 1 and 2 respectively in the following structure? -CU CECH A. B sp,sp? sp, sp sp, sp sp', sp sp, sp Ans. 2. What is the IUPAC name for the molecule shown below? os B. C. D. E. (E)-5-methyl-5-hepten-1-yne (2)-5-methyl-5-hepten-1-yne (E)-3-methyl-2-hepten-6-yne (2)-3-methyl-2-hepten-6-yne...
Draw the major product formed when the following epoxide reacts
with methanol in the presence of sulfuric acid. Use wedge/dash
bonds, including H\'s at each stereogenic center, to show the
stereochemistry of the product.
References) Draw the structure of the bromohydrin formed when (E)-3-methyl-3-hexene reacts with Br2/H20. Use the wedge/hash bond tools to indicate stereochemistry where it exists. If the reaction produces a racemic mixture, draw both stereoisomers. Separate multiple products using the + sign from the drop-down menu. е CH3 H,с Br CHy ChemDoodle ChemDoodle"
The tosylate of (2R, 3R)-3-phenylbutan-2-ol undergoes an E2 elimination on treatment with sodium ethoxide. Draw the structure of the alkene that is produced. Use the wedge hash bond tools to indicate stereochemistry. You do not have to explicitly draw H atoms. If a group is achiral, do not me wedged or hashed bonds on it. Predict the major alkene product of the following E1 reaction: Amines are converted into alkene5, by a two-step process called the Hofmann elimination. S_N 2...
6) Draw the structure of (Z)-1-chloro-2-methyl-2-butene. 7) Draw the curved arrows to show how CH3CH=CHCH2CH3 reacts with HBr to form a carbocation first, and then forms 2-bromopentane. (this is 2 steps) 7) 8) 8) Predict the product(s) of the following reaction based on the curved arrows: Make sure to include + and- charges where appropriate. -C-NH2 CH CHy HO 9) Based on the following reaction coordinate diagram: Which compound, A or C, is formed faster from B? Which is more...
Draw the structure(s) of the major organic product(s) of the following reaction, omitting the phosphine oxide. + 2 H2C=PPhg H H • You do not have to consider stereochemistry • li no reaction occurs, draw the organic starting material. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner • Separate multiple products using the + sign from the drop-down menu. P wat opy A (C4H100) reacts with phosphorus tribromide to give...
Which of the following correctly reflects relative stabilities of carbocations? 3 degree allylic > 2 degree > 1 degree benzylic methyl > 2 degree benzylic > 3 degree 3 degree benzylic > vinyl >1 degree 2 degree allylic > 2 degree > vinyl 1 degree benzylic > 3 degree > 3 degree allylic Dehydrohalogenation of 2-bromobutane in the presence of a strong base proceeds via which of the following mechanistic pathways? S_N1 S_N2 E1 E2 none of the above Which...
please help me with questions from 3-10! and the bonus.
thank you so much
Directions: Place your answers to the following questions in the provided spaces. (12 PTS) 1. What is the hybridization of the carbon atoms numbered 1 and 2 respectively in the following structure? -CU CECH A. B sp,sp? sp, sp sp, sp sp', sp sp, sp Ans. 2. What is the IUPAC name for the molecule shown below? os B. C. D. E. (E)-5-methyl-5-hepten-1-yne (2)-5-methyl-5-hepten-1-yne (E)-3-methyl-2-hepten-6-yne (2)-3-methyl-2-hepten-6-yne...
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