full question is given in all the picture. please please be clear and precise. I need help asap. the hw is due in few hours please.
Homework Answers
1. Answers in sequence from first to last blank : E, E2, F, Anti-periplanar, cis.
2. Answers in sequence from first to last blank : D, E, F, SN1, E1, Intermediate Carbocation Formation, B, C, E.
![H20:20 END OH2 Pure Н H₂O Extra step H6+ Ho Carbocation intermediate ors good leaving group H2O Es OH S1 (D) [ ] mixture of t](http://img.homeworklib.com/questions/8f8fe1d0-71b8-11ea-88ac-af4fc7d4e3fc.png?x-oss-process=image/resize,w_560)
In the second case, the other
product here could be A, instead of
B. But A itself is the reactant.
So we cannot include that in products. Again, F
cannot be the product either, as we need the formation of the
Carbocation intermediate for that(since F cannot
be formed by E2 elimination). And lastly, B and
C are diastereomers, but since they are not formed
in equal amounts as an appropriate mixture, we did not represent
them both by one structure, namely D.
3. Answers in sequence from first to last blank : J, SN2, C, Base Catalysed Ester Hydrolysis.
Add Answer to:
full question is given in all the picture. please
please be clear and precise. I need...
OTs Reagent OTs OH OH OH OH OH OH Look at the given reaction and use...
OTs Reagent OTs OH OH OH OH OH OH Look at the given reaction and use the letter code corresponding to each compound in the blank to indicate the expected products) or correct vocabulary word/phrase to complete the description. If a specific stereoisomer (e.g single enantiomer) is formed, select that isomer only. If a mixture of stereoisomers (e.g. racemic or diastereomers) is formed, select the single structure that shows the appropriate mixture (e.g. lines not dashes). If we used the...
Look at the given reaction and use the letter code corresponding to each compound in the...
Look at the given reaction and use the letter code corresponding to each compound in the blank to indicate the expected product(s), or fill in the blank with the appropriate vocabulary word or phrase. If a specific stereoisomer (e.g., single enantiomer) is formed, select that isomer only. If a mixture of stereoisomers (e.g. racemic or diastereomers) is formed, select the single structure that shows the appropriate mixture (e.g. lines not dashes). The specific functional group in the starting material is...
10. Please Check 1 by 1 and read carefully. I would need a perfect score for...
10.
Please Check 1 by 1 and read carefully. I would need a perfect
score for this . Thanks
Select the keyword or phrase that will best complete each sentence A Claisen reaction is a nucleophilic substitution in which an enolate is the nucleophile Key terms: Robinson annulation Aldol condensation: An aldol reaction in which the initially formed p hydroxyl carbonyl compound loses water by dehydration. Claisen reaction Aldol condensation Dieckmann reaction: An intramolecular Claisen reaction of a diester to...
is my answer right? university or com p any Br H2O Y Mom ??? OH S...
is my answer right?
university or com p any Br H2O Y Mom ??? OH S Port to ă Toth ♡ ♡ Tu Y Look at the given reaction and use the letter code corresponding to each compound in the blank to indicate the expected product(s). If a specific stereoisomer (e.g single enantiomer) is formed, select that isomer only. If a mixture of stereoisomers (e.g. racemic or diastereomers) is formed, select the single structure that shows the appropriate mixture (e.g....
Dropdown Menus: 1. methyl, primary (unhindered), primary (hindered), secondary, tertiary 2. poor, weakly basic, strongly basic...
Dropdown Menus:
1. methyl, primary (unhindered), primary (hindered), secondary,
tertiary
2. poor, weakly basic, strongly basic (hindered), strongly basic
(unhindered)
3. protic, aprotic
4. SN2, SN1, E1, E2, SN2 AND E2, SN1 AND E1, No Reaction
5. randomized, inverted, predictable but not inverted,
unchanged
6. a planar carbocation intermediate, backside attack transition
state, anti-periplanar transition state, other
OH Hom 유 용 The Tone The ♡ ♡ Tñ y OH H OH E OH F HO3 G Look at the given...
please explain the work 1. Predict the major organic product for each of the following elimination...
please explain the work
1. Predict the major organic product for each of the following elimination reactions, and indicate whether each one occurs via the E1 or the E2 mechanism. Be sure to clearly indicate the proper stereochemical relationships between groups (if appropriate), and write the word "racemic" under any compound that is formed as a racemic mixture. Br H3CY CH3 NaOCH3. CH3OH OH يلي H2SO4 ما H3c OTS KOt-Bu t-BuOH AgNO3 H20 Ph HC, NaOH H2O OH H2SO4
please explain the work for both questions please 1. Predict the major organic product for each...
please explain the work for both questions please
1. Predict the major organic product for each of the following elimination reactions, and indicate whether each one occurs via the E1 or the E2 mechanism. Be sure to clearly indicate the proper stereochemical relationships between groups (if appropriate), and write the word “racemic” under any compound that is formed as a racemic mixture. Br AgNO3 H2O KOt-Bu H3CCH3 H36Br t-BuOH OTS NaOCH3 CH3OH CH3 NaOH H20 2. Draw all possible E2...
ANSWER ALL QUESTIONS AND ALL PARTS FULLY! 1. Provide the reagent needed to convert 2-pentanol to...
ANSWER ALL QUESTIONS AND ALL PARTS FULLY!
1. Provide the reagent needed to convert 2-pentanol to 2-bromopentane (3 points). 2. Provide the reagent needed to complete the reaction below (1 point) De - Di 3. Give the products for the following reactions (6 points). нс он HCI HC on here a. OH O mot 1. NaH 2. CH CH CH(CH3)CH2CI 1, CHICAS COLGA SOCI Pyridine HBr 4. For each molecule, give the electrophile and the nucleophile that formed the compound...
For the first six blanks, please choose only options from the dropdown menus provided below the...
For the first six blanks, please choose only options from the
dropdown menus provided below the pictures.
Dropdown Menus:
1. methyl, primary (unhindered), primary (hindered), secondary,
tertiary
2. poor, weakly basic, strongly basic (hindered), strongly basic
(unhindered)
3. protic, aprotic
4. SN2, SN1, E1, E2, SN2 AND E2, SN1 AND E1, No Reaction
5. randomized, inverted, predictable but not inverted,
unchanged
6. a planar carbocation intermediate, backside attack transition
state, anti-periplanar transition state, other
CH3OH ~ ??? Br - în...
Please answer all 3 and explain if you can! Thank you!! *This one isn't option 2...
Please answer all 3 and explain if you can! Thank you!!
*This one isn't option 2 or 4*
Draw the major organic products of the following reaction. Include lone pairs of electrons and stereochemistry 1.CH,MgBr, Et,o 2. H,O What is the major product in the following series of reactions? 1) 03 then DMS 2) LiAIH4 (excess) then H20 3) NaH (1 equiv.) 4) TsCl (1 equiv.) 5) NaOH (dilute) Products OTS a) b) HO HO OTS он OH c) d)...
OTs Reagent OTs OH OH OH OH OH OH Look at the given reaction and use the letter code corresponding to each compound in the blank to indicate the expected products) or correct vocabulary word/phrase to complete the description. If a specific stereoisomer (e.g single enantiomer) is formed, select that isomer only. If a mixture of stereoisomers (e.g. racemic or diastereomers) is formed, select the single structure that shows the appropriate mixture (e.g. lines not dashes). If we used the...
Look at the given reaction and use the letter code corresponding to each compound in the blank to indicate the expected product(s), or fill in the blank with the appropriate vocabulary word or phrase. If a specific stereoisomer (e.g., single enantiomer) is formed, select that isomer only. If a mixture of stereoisomers (e.g. racemic or diastereomers) is formed, select the single structure that shows the appropriate mixture (e.g. lines not dashes). The specific functional group in the starting material is...
10.
Please Check 1 by 1 and read carefully. I would need a perfect
score for this . Thanks
Select the keyword or phrase that will best complete each sentence A Claisen reaction is a nucleophilic substitution in which an enolate is the nucleophile Key terms: Robinson annulation Aldol condensation: An aldol reaction in which the initially formed p hydroxyl carbonyl compound loses water by dehydration. Claisen reaction Aldol condensation Dieckmann reaction: An intramolecular Claisen reaction of a diester to...
is my answer right?
university or com p any Br H2O Y Mom ??? OH S Port to ă Toth ♡ ♡ Tu Y Look at the given reaction and use the letter code corresponding to each compound in the blank to indicate the expected product(s). If a specific stereoisomer (e.g single enantiomer) is formed, select that isomer only. If a mixture of stereoisomers (e.g. racemic or diastereomers) is formed, select the single structure that shows the appropriate mixture (e.g....
Dropdown Menus:
1. methyl, primary (unhindered), primary (hindered), secondary,
tertiary
2. poor, weakly basic, strongly basic (hindered), strongly basic
(unhindered)
3. protic, aprotic
4. SN2, SN1, E1, E2, SN2 AND E2, SN1 AND E1, No Reaction
5. randomized, inverted, predictable but not inverted,
unchanged
6. a planar carbocation intermediate, backside attack transition
state, anti-periplanar transition state, other
OH Hom 유 용 The Tone The ♡ ♡ Tñ y OH H OH E OH F HO3 G Look at the given...
please explain the work
1. Predict the major organic product for each of the following elimination reactions, and indicate whether each one occurs via the E1 or the E2 mechanism. Be sure to clearly indicate the proper stereochemical relationships between groups (if appropriate), and write the word "racemic" under any compound that is formed as a racemic mixture. Br H3CY CH3 NaOCH3. CH3OH OH يلي H2SO4 ما H3c OTS KOt-Bu t-BuOH AgNO3 H20 Ph HC, NaOH H2O OH H2SO4
please explain the work for both questions please
1. Predict the major organic product for each of the following elimination reactions, and indicate whether each one occurs via the E1 or the E2 mechanism. Be sure to clearly indicate the proper stereochemical relationships between groups (if appropriate), and write the word “racemic” under any compound that is formed as a racemic mixture. Br AgNO3 H2O KOt-Bu H3CCH3 H36Br t-BuOH OTS NaOCH3 CH3OH CH3 NaOH H20 2. Draw all possible E2...
ANSWER ALL QUESTIONS AND ALL PARTS FULLY!
1. Provide the reagent needed to convert 2-pentanol to 2-bromopentane (3 points). 2. Provide the reagent needed to complete the reaction below (1 point) De - Di 3. Give the products for the following reactions (6 points). нс он HCI HC on here a. OH O mot 1. NaH 2. CH CH CH(CH3)CH2CI 1, CHICAS COLGA SOCI Pyridine HBr 4. For each molecule, give the electrophile and the nucleophile that formed the compound...
For the first six blanks, please choose only options from the
dropdown menus provided below the pictures.
Dropdown Menus:
1. methyl, primary (unhindered), primary (hindered), secondary,
tertiary
2. poor, weakly basic, strongly basic (hindered), strongly basic
(unhindered)
3. protic, aprotic
4. SN2, SN1, E1, E2, SN2 AND E2, SN1 AND E1, No Reaction
5. randomized, inverted, predictable but not inverted,
unchanged
6. a planar carbocation intermediate, backside attack transition
state, anti-periplanar transition state, other
CH3OH ~ ??? Br - în...
Please answer all 3 and explain if you can! Thank you!!
*This one isn't option 2 or 4*
Draw the major organic products of the following reaction. Include lone pairs of electrons and stereochemistry 1.CH,MgBr, Et,o 2. H,O What is the major product in the following series of reactions? 1) 03 then DMS 2) LiAIH4 (excess) then H20 3) NaH (1 equiv.) 4) TsCl (1 equiv.) 5) NaOH (dilute) Products OTS a) b) HO HO OTS он OH c) d)...
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