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For number 8 I know the answer is B but I don’t know why it’s
not...
7. Predict the product(s) of each of the following reactions include stereochemistry where important and indicate...
7. Predict the product(s) of each of the following reactions include stereochemistry where important and indicate the mechanism (S, S,2, El, E2). 80°C a 2-chloro-2-methylbutane NaOH Н.о b. (R)-2-chloropentane Nac c-H DMSO с1 (снс. Cн, CH,ОН d. trans-1-chloro-3-methylcyclohexane+ NaOC(CH) e. 2-chloro-3-phenylbutane Н.о f. trans-1-bromo-3-methyleyclopentane Nal acetone NaOCH THон g 2-chloro-2-methylbutane EIOH h R-3-bromo-2-methylpentane . trans-1-bromo-2-isopropyleyclohexane CHCOK NaSH Н,о j. 1-bromopropaе NaOCH снон CH коссH). I-bromobutane m. cis-1-chloro-3-methyleyclobutane Nal DMSO сHсH,он n. (R)-2-iodo-2-phenylethane NaOH o. 1-iodobutane p. 2-bromo-3-methylbutane KOC(CH). но (S)-3-chlorocyclopentene...
1. a) Complete the balanced net ionic equation for these nucleophilic substitution reactions. b) State whether e...
1. a) Complete the balanced net ionic equation for these nucleophilic substitution reactions. b) State whether each reaction will occur by Sn1 or Sn2 mechanisms ma + o CH₃ H3C-50 + Y Z-I + CH3OH I Br + H2O 2. Which compound in the following pairs will react fast nd in the following pairs will react faster in an SN2 reaction? Give a reason why. a) 1 bromobutane or 2-bromobutane b) 2-bromo-2-methylpentane or 2-bromo-4-methylpentane? c) 1-chlorohexane or chlorocyclohexane? d) chloromethane...
I think it’s B. Please let me know if it’s B or C? ADEDUUR Enthalpy of...
I think it’s B. Please let me know if it’s B or C?
ADEDUUR Enthalpy of Electrophilic Aromatic Substitution Homework . Unanswered Due in 18 hours Which of the following statements is true about the mechanism of electrophilic aromatic substitution. O A The first step (addition) is exothermic and the second step (elimination) is exothermic. B The first step (addition) is exothermic and the second step (elimination) is endothermic. O c The first step (addition) is endothermic and the second...
the answers i circled are incorrect except for 13. i know 11 is d and 15 is a. can you please explain why these three a...
the answers i circled are incorrect except for 13. i know 11
is d and 15 is a. can you please explain why these three are
correct as well. can you give me the correct answers and explain
why?
de motor and h ow w generation recognized disorder that can benefit from hippothy wy b o cice to which they were anached indiactive donation of electron density to the cationic center chan inductive removal of electron density from the w...
Helerences Reagents Available a. H20, H2SO4. HgSO4 f. H2, Lindlar catalyst b. BH3 then H2O2 g....
Helerences Reagents Available a. H20, H2SO4. HgSO4 f. H2, Lindlar catalyst b. BH3 then H2O2 g. Li, NH3 (lia) c. NaNH2 h. CH2lz, Zn(Cu) d. CH3CH2Br i. H2, Pd/C e. HCl, ether j. Br2, CH2Cl2 Select reagents from the above table to carry out each of the following reactions If only a single step is required, select (none) from the drop down list CH2CH2CH2C=CCH3 C H2CH2CH2CH2CH2CH3 Reaction 1 Step 1: Step 2: CH3CH2CH2C=CH CHCH2CH2CH3 Reaction 2 Step 1: Step 2:...
i need help with problem 3 and the included questions that are apart of it attached...
i need help with problem 3 and the included questions that are
apart of it attached below
a.)Using curved arrows, draw the stepwise mechanism for the
reaction that begins with reactant (a) in the question above.Be
sure to draw each intermediate, including any charges.
b.). Using curved arrows, draw the stepwise mechanism for the
reaction that forms product (d) in the question above. Be sure to
draw each intermediate, including any charges.
c.)Using curved arrows, draw the stepwise mechanism for...
Reagents Available a. H20, H2SO4, HgSO4 b. BH3 then H202 c. NANH2 d. CH3CH2Br e. HCI,...
Reagents Available a. H20, H2SO4, HgSO4 b. BH3 then H202 c. NANH2 d. CH3CH2Br e. HCI, ether f. H2, Lindlar catalyst g. Li, NH3 (ia) h. CH2l2, Zn(Cu) i. H2, Pd/C 1. Вrz. СH2Cl Select reagents from the above table to carry out each of the following reactions. If only a single step is required, select (none) from the drop down list. ? CH-CH-CH2C3CСН3 CH,CH-CH2CH2CH-CHз Reaction 1: Step 1: G Step 2: 0 CH3CH2CH2C CH CH,CH2CH2CH2CНО t Reaction 2: Step...
I really don’t understand number three. I know why it is irreducible. But I don’t know...
I really don’t understand number three. I know why it is
irreducible. But I don’t know how to do the rest of it. And since I
can’t do three I can’t do four. And since I can’t before I cant do
five. help me please.
Show that QV2): Q1 3. (We ve looked at uus previoes 2. [Q(Vz, 3): Q(V2)] = 2. Q(2) and use it to show that Explain why x2 +3 is irreducible over 3. Then, apply the...
i am done with mine but i do need an answer key to check my work....
i am done with mine but i do need an answer key to check my work.
can you help? thank you
Organic Chemistry I Worksheet Due 10/28/19 Predict the alkene product or products formed by sodium methoxide [NaOCHs] promoted dehydrohalogenation (- HX) of the following compounds. In each case, predict which product will be the major product. 1. 2-bromobutane A. 3-chloropentane В. Predict the product or products formed by potassium tert-butoxide [KOC(CH3)s] promoted dehydrohalogenation of the following compounds. In each...
7. Predict the product(s) of each of the following reactions include stereochemistry where important and indicate the mechanism (S, S,2, El, E2). 80°C a 2-chloro-2-methylbutane NaOH Н.о b. (R)-2-chloropentane Nac c-H DMSO с1 (снс. Cн, CH,ОН d. trans-1-chloro-3-methylcyclohexane+ NaOC(CH) e. 2-chloro-3-phenylbutane Н.о f. trans-1-bromo-3-methyleyclopentane Nal acetone NaOCH THон g 2-chloro-2-methylbutane EIOH h R-3-bromo-2-methylpentane . trans-1-bromo-2-isopropyleyclohexane CHCOK NaSH Н,о j. 1-bromopropaе NaOCH снон CH коссH). I-bromobutane m. cis-1-chloro-3-methyleyclobutane Nal DMSO сHсH,он n. (R)-2-iodo-2-phenylethane NaOH o. 1-iodobutane p. 2-bromo-3-methylbutane KOC(CH). но (S)-3-chlorocyclopentene...
1. a) Complete the balanced net ionic equation for these nucleophilic substitution reactions. b) State whether each reaction will occur by Sn1 or Sn2 mechanisms ma + o CH₃ H3C-50 + Y Z-I + CH3OH I Br + H2O 2. Which compound in the following pairs will react fast nd in the following pairs will react faster in an SN2 reaction? Give a reason why. a) 1 bromobutane or 2-bromobutane b) 2-bromo-2-methylpentane or 2-bromo-4-methylpentane? c) 1-chlorohexane or chlorocyclohexane? d) chloromethane...
I think it’s B. Please let me know if it’s B or C?
ADEDUUR Enthalpy of Electrophilic Aromatic Substitution Homework . Unanswered Due in 18 hours Which of the following statements is true about the mechanism of electrophilic aromatic substitution. O A The first step (addition) is exothermic and the second step (elimination) is exothermic. B The first step (addition) is exothermic and the second step (elimination) is endothermic. O c The first step (addition) is endothermic and the second...
the answers i circled are incorrect except for 13. i know 11
is d and 15 is a. can you please explain why these three are
correct as well. can you give me the correct answers and explain
why?
de motor and h ow w generation recognized disorder that can benefit from hippothy wy b o cice to which they were anached indiactive donation of electron density to the cationic center chan inductive removal of electron density from the w...
Helerences Reagents Available a. H20, H2SO4. HgSO4 f. H2, Lindlar catalyst b. BH3 then H2O2 g. Li, NH3 (lia) c. NaNH2 h. CH2lz, Zn(Cu) d. CH3CH2Br i. H2, Pd/C e. HCl, ether j. Br2, CH2Cl2 Select reagents from the above table to carry out each of the following reactions If only a single step is required, select (none) from the drop down list CH2CH2CH2C=CCH3 C H2CH2CH2CH2CH2CH3 Reaction 1 Step 1: Step 2: CH3CH2CH2C=CH CHCH2CH2CH3 Reaction 2 Step 1: Step 2:...
i need help with problem 3 and the included questions that are
apart of it attached below
a.)Using curved arrows, draw the stepwise mechanism for the
reaction that begins with reactant (a) in the question above.Be
sure to draw each intermediate, including any charges.
b.). Using curved arrows, draw the stepwise mechanism for the
reaction that forms product (d) in the question above. Be sure to
draw each intermediate, including any charges.
c.)Using curved arrows, draw the stepwise mechanism for...
Reagents Available a. H20, H2SO4, HgSO4 b. BH3 then H202 c. NANH2 d. CH3CH2Br e. HCI, ether f. H2, Lindlar catalyst g. Li, NH3 (ia) h. CH2l2, Zn(Cu) i. H2, Pd/C 1. Вrz. СH2Cl Select reagents from the above table to carry out each of the following reactions. If only a single step is required, select (none) from the drop down list. ? CH-CH-CH2C3CСН3 CH,CH-CH2CH2CH-CHз Reaction 1: Step 1: G Step 2: 0 CH3CH2CH2C CH CH,CH2CH2CH2CНО t Reaction 2: Step...
I really don’t understand number three. I know why it is
irreducible. But I don’t know how to do the rest of it. And since I
can’t do three I can’t do four. And since I can’t before I cant do
five. help me please.
Show that QV2): Q1 3. (We ve looked at uus previoes 2. [Q(Vz, 3): Q(V2)] = 2. Q(2) and use it to show that Explain why x2 +3 is irreducible over 3. Then, apply the...
i am done with mine but i do need an answer key to check my work.
can you help? thank you
Organic Chemistry I Worksheet Due 10/28/19 Predict the alkene product or products formed by sodium methoxide [NaOCHs] promoted dehydrohalogenation (- HX) of the following compounds. In each case, predict which product will be the major product. 1. 2-bromobutane A. 3-chloropentane В. Predict the product or products formed by potassium tert-butoxide [KOC(CH3)s] promoted dehydrohalogenation of the following compounds. In each...
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