![Question #10 [10 pts] Answer the following questions Which hydrogen is more acidic sp3GH or sp C-H·Ansseern/ NaH is a strong base or strong nucleophile? Ans: a. -Strang b. c. Show the intermediate and product in the following two step reaction. I. Nall Hl 2. CH CIH,Br](http://img.homeworklib.com/questions/b4282a60-7a24-11eb-9b49-f5eadab68ad2.png?x-oss-process=image/resize,w_560)
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Here you have asked for b and
c. So I answered only those two.Add Answer to:
b and c please
Question #10 [10 pts] Answer the following questions Which hydrogen is more...
please answer questions 1-4 Question 1 Which of the following is the most stable carbocation? СН3...
please answer questions 1-4
Question 1 Which of the following is the most stable carbocation? СН3 V. CH2 What is the major product of the following reaction? Н HBO C CHS CH CH CH3-CH ( CH, Br CH2-CH-C–CH, Br Br CH CH CH3-CH:-¢-CH Br ін, CHE CH CH.-CH- Br CH. D Question 3 What is the major product of the following reaction? CH, НО 1 Оснок IV. CH2OH CH3 "О" ОН Д. он СН3 CH3 Но Ш. CH, ОН Question...
ndyla S Chapter 7 (Snl-Sn2-E1-E2) Revie w +Problems 1°Leaving group (example): Br React with the following...
ndyla S Chapter 7 (Snl-Sn2-E1-E2) Revie w +Problems 1°Leaving group (example): Br React with the following reagents (Strong base /strong nucleophile) B) I, NC, Na (Strong nucleophile/ weak base) C) H (NaH or Ca) tBuO/tBuOH (Strong base/non- nucleophile) D) H:0, ROH, RCO2H Weak nucleophile/ very weak base- even acidie "Solvolysis" - type reactions P 2010 2° Leaving group (example): (sometimes "hindered") Ri React with the following reagents (Strong base / strong nucleophile) B) I, NC. N (Strong nucleophile/ weak base)...
please answer questions 9-12 Question 9 1 pts Which of the following statements describes the reactivity...
please answer questions 9-12
Question 9 1 pts Which of the following statements describes the reactivity of alkynes? An alkyne is an electron-rich molecule and therefore reacts as a nucleophile. When a symmetrical internal alkyne reacts with HBr, two products are formed. Unlike alkenes, alkynes fail to undergo electrophilic addition reactions The o bonds of alkynes are greater in energy than the rt bonds and, therefore, are more reactive Alkynes react as electrophiles, whereas alkenes react as nucleophiles What is...
please answer all of the following questions. 1. [03 pts. For the following reaction, label the...
please answer all of the following questions.
1. [03 pts. For the following reaction, label the nucleophile, electrophile, and leaving group. nucleophile" Lexleasing group 2. [03 pts. Rank the following substrates from most to least reactive in an S2 reaction. 3. [02 pts.) Which of the following is the reaction diagram for endothermic Sn2 reaction? Xo 4. [03 pts.] Draw the major product for the following Sn2 reaction. NaCN 5. [02 pts.) Which reaction in the following pair takes place...
Tulung ate n illud aludke place in a single step. In the Sn2 reaction, the nucleophile...
Tulung ate n illud aludke place in a single step. In the Sn2 reaction, the nucleophile attacks the a-carbon from the backside and displaces the leaving group with an inversion of configuration occurring at the carbon. In the E2 elimination reaction, strong base removes an acidic hydrogen from the B-carbon and an alkene is formed as the leaving group is expelled from the a-carbon. This elimination follows Zaitsey's rule whereby the more substituted alkene is generally formed. In E2 elimination,...
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...
Please answer all 3 questions QUESTION What is the major product of the following reaction? 8R...
Please answer all 3 questions
QUESTION What is the major product of the following reaction? 8R QUESTION 2 From the data given in the right-hand box, what is the specific rotation, (alp, of the alcohol produced in the Sy2 reaction shown below? H H гон OH Сонуснан, HOCHE CECH CH Br Cotia lale -99 lalo = ? lalo = -34.6 34,6 -9.9 0.0 -9.9 QUESTION 3 Which of the following best describes the reaction of sodium metal with methanol to...
please answer all of the following questions. 02 pts.] Briefly explain why the following reaction yields...
please answer all of the following questions.
02 pts.] Briefly explain why the following reaction yields the Hofmann product exclusively even though the base is not sterically hindered: This is breause Br is a jood Ieavng Br CH,CH2ONa oup on q dcarloon. CH,CH,он [02 pts.] Draw the structure of alkyl that will undergo an E2 elimination to yield only the indicated alkene. CHyCHONa CHсH,он [04 pts.] Draw only the major product for each of the following elimination reactions. сн-сH,ON CнH-CHон...
48. Use the figure below to answer the following questions. TS.Cyelle nucleotide RNA 0 0 B...
48. Use the figure below to answer the following questions. TS.Cyelle nucleotide RNA 0 0 B O-POCHO 0 Н M 31 H NIE 0 HO 1 NH -0 H0 CH Ване ANI OPO H His 119 His 119 он -O-P- CH, 0-11 OPO 0- His 119 a. In the first step of the reaction. His 12 is acting as a and His 119 is acting as a a. General base, general acid b. General acid, general base c. Nucleophile, electrophile...
9. For the compound below answer a b and c. a) b) c) (3 pts) is...
9. For the compound below answer a b and c. a) b) c) (3 pts) is the molecule below an aromatic or anti-aromatic estem? (4 pts) How many electrons are in the aromatic anti aromatic bratem? (4 pts). Draw an arrow () to the lone pair electron(s) that are part of the aromatic (or anti-aromatic) system. 10. (18 pts-6 pts each) Fill in the major organic product(s) for the reactions below Br+FeBr ci + CH CH CH .. 3+ AICI:...
please answer questions 1-4
Question 1 Which of the following is the most stable carbocation? СН3 V. CH2 What is the major product of the following reaction? Н HBO C CHS CH CH CH3-CH ( CH, Br CH2-CH-C–CH, Br Br CH CH CH3-CH:-¢-CH Br ін, CHE CH CH.-CH- Br CH. D Question 3 What is the major product of the following reaction? CH, НО 1 Оснок IV. CH2OH CH3 "О" ОН Д. он СН3 CH3 Но Ш. CH, ОН Question...
ndyla S Chapter 7 (Snl-Sn2-E1-E2) Revie w +Problems 1°Leaving group (example): Br React with the following reagents (Strong base /strong nucleophile) B) I, NC, Na (Strong nucleophile/ weak base) C) H (NaH or Ca) tBuO/tBuOH (Strong base/non- nucleophile) D) H:0, ROH, RCO2H Weak nucleophile/ very weak base- even acidie "Solvolysis" - type reactions P 2010 2° Leaving group (example): (sometimes "hindered") Ri React with the following reagents (Strong base / strong nucleophile) B) I, NC. N (Strong nucleophile/ weak base)...
please answer questions 9-12
Question 9 1 pts Which of the following statements describes the reactivity of alkynes? An alkyne is an electron-rich molecule and therefore reacts as a nucleophile. When a symmetrical internal alkyne reacts with HBr, two products are formed. Unlike alkenes, alkynes fail to undergo electrophilic addition reactions The o bonds of alkynes are greater in energy than the rt bonds and, therefore, are more reactive Alkynes react as electrophiles, whereas alkenes react as nucleophiles What is...
please answer all of the following questions.
1. [03 pts. For the following reaction, label the nucleophile, electrophile, and leaving group. nucleophile" Lexleasing group 2. [03 pts. Rank the following substrates from most to least reactive in an S2 reaction. 3. [02 pts.) Which of the following is the reaction diagram for endothermic Sn2 reaction? Xo 4. [03 pts.] Draw the major product for the following Sn2 reaction. NaCN 5. [02 pts.) Which reaction in the following pair takes place...
Tulung ate n illud aludke place in a single step. In the Sn2 reaction, the nucleophile attacks the a-carbon from the backside and displaces the leaving group with an inversion of configuration occurring at the carbon. In the E2 elimination reaction, strong base removes an acidic hydrogen from the B-carbon and an alkene is formed as the leaving group is expelled from the a-carbon. This elimination follows Zaitsey's rule whereby the more substituted alkene is generally formed. In E2 elimination,...
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...
Please answer all 3 questions
QUESTION What is the major product of the following reaction? 8R QUESTION 2 From the data given in the right-hand box, what is the specific rotation, (alp, of the alcohol produced in the Sy2 reaction shown below? H H гон OH Сонуснан, HOCHE CECH CH Br Cotia lale -99 lalo = ? lalo = -34.6 34,6 -9.9 0.0 -9.9 QUESTION 3 Which of the following best describes the reaction of sodium metal with methanol to...
please answer all of the following questions.
02 pts.] Briefly explain why the following reaction yields the Hofmann product exclusively even though the base is not sterically hindered: This is breause Br is a jood Ieavng Br CH,CH2ONa oup on q dcarloon. CH,CH,он [02 pts.] Draw the structure of alkyl that will undergo an E2 elimination to yield only the indicated alkene. CHyCHONa CHсH,он [04 pts.] Draw only the major product for each of the following elimination reactions. сн-сH,ON CнH-CHон...
48. Use the figure below to answer the following questions. TS.Cyelle nucleotide RNA 0 0 B O-POCHO 0 Н M 31 H NIE 0 HO 1 NH -0 H0 CH Ване ANI OPO H His 119 His 119 он -O-P- CH, 0-11 OPO 0- His 119 a. In the first step of the reaction. His 12 is acting as a and His 119 is acting as a a. General base, general acid b. General acid, general base c. Nucleophile, electrophile...
9. For the compound below answer a b and c. a) b) c) (3 pts) is the molecule below an aromatic or anti-aromatic estem? (4 pts) How many electrons are in the aromatic anti aromatic bratem? (4 pts). Draw an arrow () to the lone pair electron(s) that are part of the aromatic (or anti-aromatic) system. 10. (18 pts-6 pts each) Fill in the major organic product(s) for the reactions below Br+FeBr ci + CH CH CH .. 3+ AICI:...
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