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H D) Suggest a method to efficiently synthesize each of the following molecules from an alkene using the reactions....
2) Order the following alkenes from most stable to least stable Нас Нас с-сн, н,с Hас +C- Нас н CHs -CH3 H Hе mos...
2) Order the following alkenes from most stable to least stable Нас Нас с-сн, н,с Hас +C- Нас н CHs -CH3 H Hе most stable least stable (a) I (b) I (c) I ll (d) 7) Order the following C-H bonds from strongest to weakest. strongest weakest (a) (b) (c) II (d) 8) Which of the following is represents the lowest energy transition state for the addition of BH, to 2-methyl-1-propene? quCH «сHs нСи Нас (b) (a) Нив--н H H...
Question 2: Determine in the following examples if the base is strong enough to deprotonate the...
Question 2: Determine in the following examples if the base is strong enough to deprotonate the terminal alkyne. сH, нс. t-BuOK + Cн Question 3: A terminal alkyne is prepared by treating the dihalide with excess (xs) sodium amide, followed by water. Predict the major product and draw a mechanism for its formation: Br 1) xs NaNHNH 2) Hо Br Identify reagents that you could use to achieve the following transformations: CH3 Нас Н,с CH3 CH3 HyC Н.с CHs CH3...
7. Synthesis Problem (15 points) Show how you would synthesize 3 of the 4 following compounds...
7. Synthesis Problem (15 points) Show how you would synthesize 3 of the 4 following compounds in one chemical reaction. You may use any starting material you wish and any organic and inorganic reagents. Clearly indicate which ones you want graded by circling the molecules н, осн, Br ОН
1. Select the best reagent(s) from the list below to accomplish the following transformations. In some...
1. Select the best reagent(s) from the list below to accomplish the following transformations. In some cases, more than one reagent may be required. 3. HSO3(aq) A.HCI B. Br? C. Hg(OAc)/H20 D. BH3 E. H30*/Hz0 E. Hz02 G. Os04 H. Brz/Hz0 NaBH4 J. H2O, in aq NaOH Reagent(s)? NaHSO3 Product CH3 Starting Material сн. Н.c = — сна BR — Br Br CH₂ На сна нс сна HC нас нас н сну нас НАС СНА оfo/Acal НО н а )...
ЕОC Problem 11.030 a. Draw the products formed when the triglyceride is saponified. Enter your answers from largest mas...
ЕОC Problem 11.030 a. Draw the products formed when the triglyceride is saponified. Enter your answers from largest mass to smallest mass. сH,(CH,),СH-CHCH), С -осн, CH2(CH)12 C OCH II CH,(CH), CH-CHCH,), С- -осн, Your answer is partially correct. Try again нс Na Edit Product 1 (largest molecular mass product) НаС Na Edit Product 2 O O O=O Edit Na Н,с. Product 3 -OH -Он Edit -OH Product 4 (smallest molecular mass product) Choose the drawings of a trans fat that...
Synthesize each of the following molecules starting with the indicated organic molecule. Each will require more...
Synthesize each of the following molecules starting with the indicated organic molecule. Each will require more than one step. Show the reagents necessary, and the product from each step of the synthesis он a. он b. C. он
Please help me with these questions,. Draw the major product of the following reaction Question 8...
Please help me with these questions,.
Draw the major product of the following reaction Question 8 н+ Нас Нас CH3 CH3 но CHзон CHз Create OscerSketch Answer 8 Incorrect: Answer has an incorrect structure. Complete the following synthesis by selecting from the list of 10 reagents below. Each reagent (or set of reagents) is labeled as a letter. In the answer box, simply place the order of reagents used as uppercase letters. For example, if your synthesis involves using reagent...
Identifying functional groups in each of the following molecules really need help with this question!! it's...
Identifying functional groups in each of the following
molecules
really need help with this question!! it's identifying
functional groups, the picture of the question is linked here:
Be sure to answer all parts. Identify and classify the functional group in each of the following molecules (select) (а) сн,CHCСH ketone (b) -о—снз Нас C (select) (c) CH2CH2NH2 CH3 (select) (d) н,с —сн, C (select) (e) CH,CH,осн,сH, он (select) CH CH Н.с (select) (g) CHCOH (select) (h) CH CH CH=CH2 (select) Н.с...
b. How will you synthesize the following compounds starting from an alkene? Draw the structure of...
b. How will you synthesize the following compounds starting from an alkene? Draw the structure of the alkene and the reagent(s) used for the synthesis. Он CH3CCH2CH2CH2CH3 CHз a. CH3 CH3CH2CHCHCH2CH3 он b. Он CH3CHCH2 C. Br 7. Draw one possible structure for the following. a. A hydrocarbon with formula CeH16, on hydrogenation, reacted with 1 molar equivalence of Hz2 (g) in presence of Pd catalyst. Draw any one possible structure. b. A hydrocarbon with formula CeH 12, on hydrogenation,...
1. (4 pts) Rank each of the following carbocations in order of stability (1 most stable...
1. (4 pts) Rank each of the following carbocations in order of stability (1 most stable and 4 least stable). н н сH н Н,с Н,с" H сH; CH3 Hас- H 2. (6 pts total; 2 pts each) Complete the following transformations by indicating the reactant structure or the major organic product(s). Place your answer(s) in the space provided. Be certain to indicate stereochemistry where applicable. Cl2 Он cat. H2SO H-о Br Br conc. HBra) сн сна 3. (10 pts...
2) Order the following alkenes from most stable to least stable Нас Нас с-сн, н,с Hас +C- Нас н CHs -CH3 H Hе most stable least stable (a) I (b) I (c) I ll (d) 7) Order the following C-H bonds from strongest to weakest. strongest weakest (a) (b) (c) II (d) 8) Which of the following is represents the lowest energy transition state for the addition of BH, to 2-methyl-1-propene? quCH «сHs нСи Нас (b) (a) Нив--н H H...
Question 2: Determine in the following examples if the base is strong enough to deprotonate the terminal alkyne. сH, нс. t-BuOK + Cн Question 3: A terminal alkyne is prepared by treating the dihalide with excess (xs) sodium amide, followed by water. Predict the major product and draw a mechanism for its formation: Br 1) xs NaNHNH 2) Hо Br Identify reagents that you could use to achieve the following transformations: CH3 Нас Н,с CH3 CH3 HyC Н.с CHs CH3...
7. Synthesis Problem (15 points) Show how you would synthesize 3 of the 4 following compounds in one chemical reaction. You may use any starting material you wish and any organic and inorganic reagents. Clearly indicate which ones you want graded by circling the molecules н, осн, Br ОН
1. Select the best reagent(s) from the list below to accomplish the following transformations. In some cases, more than one reagent may be required. 3. HSO3(aq) A.HCI B. Br? C. Hg(OAc)/H20 D. BH3 E. H30*/Hz0 E. Hz02 G. Os04 H. Brz/Hz0 NaBH4 J. H2O, in aq NaOH Reagent(s)? NaHSO3 Product CH3 Starting Material сн. Н.c = — сна BR — Br Br CH₂ На сна нс сна HC нас нас н сну нас НАС СНА оfo/Acal НО н а )...
ЕОC Problem 11.030 a. Draw the products formed when the triglyceride is saponified. Enter your answers from largest mass to smallest mass. сH,(CH,),СH-CHCH), С -осн, CH2(CH)12 C OCH II CH,(CH), CH-CHCH,), С- -осн, Your answer is partially correct. Try again нс Na Edit Product 1 (largest molecular mass product) НаС Na Edit Product 2 O O O=O Edit Na Н,с. Product 3 -OH -Он Edit -OH Product 4 (smallest molecular mass product) Choose the drawings of a trans fat that...
Synthesize each of the following molecules starting with the indicated organic molecule. Each will require more than one step. Show the reagents necessary, and the product from each step of the synthesis он a. он b. C. он
Please help me with these questions,.
Draw the major product of the following reaction Question 8 н+ Нас Нас CH3 CH3 но CHзон CHз Create OscerSketch Answer 8 Incorrect: Answer has an incorrect structure. Complete the following synthesis by selecting from the list of 10 reagents below. Each reagent (or set of reagents) is labeled as a letter. In the answer box, simply place the order of reagents used as uppercase letters. For example, if your synthesis involves using reagent...
Identifying functional groups in each of the following
molecules
really need help with this question!! it's identifying
functional groups, the picture of the question is linked here:
Be sure to answer all parts. Identify and classify the functional group in each of the following molecules (select) (а) сн,CHCСH ketone (b) -о—снз Нас C (select) (c) CH2CH2NH2 CH3 (select) (d) н,с —сн, C (select) (e) CH,CH,осн,сH, он (select) CH CH Н.с (select) (g) CHCOH (select) (h) CH CH CH=CH2 (select) Н.с...
b. How will you synthesize the following compounds starting from an alkene? Draw the structure of the alkene and the reagent(s) used for the synthesis. Он CH3CCH2CH2CH2CH3 CHз a. CH3 CH3CH2CHCHCH2CH3 он b. Он CH3CHCH2 C. Br 7. Draw one possible structure for the following. a. A hydrocarbon with formula CeH16, on hydrogenation, reacted with 1 molar equivalence of Hz2 (g) in presence of Pd catalyst. Draw any one possible structure. b. A hydrocarbon with formula CeH 12, on hydrogenation,...
1. (4 pts) Rank each of the following carbocations in order of stability (1 most stable and 4 least stable). н н сH н Н,с Н,с" H сH; CH3 Hас- H 2. (6 pts total; 2 pts each) Complete the following transformations by indicating the reactant structure or the major organic product(s). Place your answer(s) in the space provided. Be certain to indicate stereochemistry where applicable. Cl2 Он cat. H2SO H-о Br Br conc. HBra) сн сна 3. (10 pts...
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