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-OH Give products and type of mechanism H₂SO4 -CH3 120°C, distill KON CH₂ - CH₂ CH3 acetone 20°C OTS CH₃COZH 3...
Give products and type of mechanism. please show all work KEN " CH₂ - CH₂ CH3...
Give products and type of mechanism. please show all work
KEN " CH₂ - CH₂ CH3 ОТ: acetone, 20% CH3CO2, В снсоон, CH3CH, он in AgNO3 mm Br
4.2 Give a detailed mechanism and show the products of the following reactions: OF CH3 C...
4.2 Give a detailed mechanism and show the products of the following reactions: OF CH3 C (6] a) C-H E2 ООCH H CHз H b) H3CC E1 CH3 Н-О Br 4.3 Label the following reactions as SN1, SN2, E1, or E2. . Br NaNH2 THE a) HN CI КОН Ethanol b) но Ethanol c) NaOH Ethanol P OH 4A samnle with a.concentration of 0 3 a/ml was nlaced in a cell with a lenath of 5 cm 41
GIVE PRODUCTS Ca) Cb) Cc) C PROVIDE A DETAILED MECHANISM CH 3 CH3 CH2 CH20H CH3...
GIVE PRODUCTS Ca) Cb) Cc) C PROVIDE A DETAILED MECHANISM CH 3 CH3 CH2 CH20H CH3 40°C CH 3) RANK in order of INCREASING STABILITY. ExPLAIN CH3 CH3 CH CH2
2 problems REVIEW Topics [References) CH HC OCH Br2 CH3 B H3C CH,OH H₂C CH₂ Electrophilic...
2 problems
REVIEW Topics [References) CH HC OCH Br2 CH3 B H3C CH,OH H₂C CH₂ Electrophilic addition of hypohalous acids to alkenes yields a 1,2-haloalcohol called a halohydrin. Halohydrin formation, however, does not result from the addition of HOBr, for example. Instead the addition is done indirectly by reaction of the alkene with Br, in the presence of water. The reaction also works with Cl2 to give chlorohydrins instead of bromohydrins. The reaction proceeds through a cyclic intermediate known as...
C-H bond BDE (kJ/mol) CH3-H 439 C2H:-H 422 (CH3)2 CH-H 414 (CH3)3 C-H 405 Table of...
C-H bond BDE (kJ/mol) CH3-H 439 C2H:-H 422 (CH3)2 CH-H 414 (CH3)3 C-H 405 Table of Bond Dissociation Enthalpies C-X bond BDE (kJ/mol) X2 and HX bonds BDE (kJ/mol) CH3-C1 351 CI 247 CH-C1 355 НСІ 431 (CH3)2CH-C 355 (CH3)3C-CI 355 CH3 CH3 CH3CHCHCH3 CH3CHCH2CH3 + a Cl2 CI HCI Using the table of bond dissociation energies in the first part of this question: Calculate AH for this reaction. kJ/mol Overall, this reaction is CH3 CH3CHCHCH3 CH3 CH3CHCH2CH3 + b...
1. What substitution mechanism will the following reaction likely proceed through? (1pt) CH3 HU. : N=C:...
1. What substitution mechanism will the following reaction likely proceed through? (1pt) CH3 HU. : N=C: +3C-Br - NC-C WH + Br HT 2. Label the componetns of the above reation as: Nucleophile, electrophile, leaving group (3pt) 3. Assign R and S configuration to the following reactant and products (2pt) NaOH HO + HO-COCH3 H.COwc-OH + HO-6 H2COCCI H H 4. What ratio should the two above products be formed in and what is their stereochemical relationship? (2pt) 5. Predict...
CHA CH₂ + H₂C Mai H₂C • treating 1,3-butadiene w/ one mole of HCl give a mixture ok 2 isometric products. Draw curv...
CHA CH₂ + H₂C Mai H₂C • treating 1,3-butadiene w/ one mole of HCl give a mixture ok 2 isometric products. Draw curved arrows to show the movement of electrons in this step of the rxn mechanism. ci: CH2 : > cha
4. [12 pts] Propose mechanisms for the formation of all 3 products shown in the reaction...
4. [12 pts] Propose mechanisms for the formation of all 3 products shown in the reaction below: (draw curved arrows, intermediates, and resonance structures if necessary. NO NEED FOR TRANSITION STATES! CH CH CH CH Br Heat CH,CH,OH OCH.CH Mechanism.14 points) Mechanism 2 points) Mechanism.3 14 points) 5. [14 pts] Provide the major products of reacting the alkene shown in the middle of the scheme below with all the reagents independently. Draw the products' structures in the corresponding table below...
Give products and type of mechanism. please show all work
KEN " CH₂ - CH₂ CH3 ОТ: acetone, 20% CH3CO2, В снсоон, CH3CH, он in AgNO3 mm Br
4.2 Give a detailed mechanism and show the products of the following reactions: OF CH3 C (6] a) C-H E2 ООCH H CHз H b) H3CC E1 CH3 Н-О Br 4.3 Label the following reactions as SN1, SN2, E1, or E2. . Br NaNH2 THE a) HN CI КОН Ethanol b) но Ethanol c) NaOH Ethanol P OH 4A samnle with a.concentration of 0 3 a/ml was nlaced in a cell with a lenath of 5 cm 41
GIVE PRODUCTS Ca) Cb) Cc) C PROVIDE A DETAILED MECHANISM CH 3 CH3 CH2 CH20H CH3 40°C CH 3) RANK in order of INCREASING STABILITY. ExPLAIN CH3 CH3 CH CH2
2 problems
REVIEW Topics [References) CH HC OCH Br2 CH3 B H3C CH,OH H₂C CH₂ Electrophilic addition of hypohalous acids to alkenes yields a 1,2-haloalcohol called a halohydrin. Halohydrin formation, however, does not result from the addition of HOBr, for example. Instead the addition is done indirectly by reaction of the alkene with Br, in the presence of water. The reaction also works with Cl2 to give chlorohydrins instead of bromohydrins. The reaction proceeds through a cyclic intermediate known as...
C-H bond BDE (kJ/mol) CH3-H 439 C2H:-H 422 (CH3)2 CH-H 414 (CH3)3 C-H 405 Table of Bond Dissociation Enthalpies C-X bond BDE (kJ/mol) X2 and HX bonds BDE (kJ/mol) CH3-C1 351 CI 247 CH-C1 355 НСІ 431 (CH3)2CH-C 355 (CH3)3C-CI 355 CH3 CH3 CH3CHCHCH3 CH3CHCH2CH3 + a Cl2 CI HCI Using the table of bond dissociation energies in the first part of this question: Calculate AH for this reaction. kJ/mol Overall, this reaction is CH3 CH3CHCHCH3 CH3 CH3CHCH2CH3 + b...
1. What substitution mechanism will the following reaction likely proceed through? (1pt) CH3 HU. : N=C: +3C-Br - NC-C WH + Br HT 2. Label the componetns of the above reation as: Nucleophile, electrophile, leaving group (3pt) 3. Assign R and S configuration to the following reactant and products (2pt) NaOH HO + HO-COCH3 H.COwc-OH + HO-6 H2COCCI H H 4. What ratio should the two above products be formed in and what is their stereochemical relationship? (2pt) 5. Predict...
CHA CH₂ + H₂C Mai H₂C • treating 1,3-butadiene w/ one mole of HCl give a mixture ok 2 isometric products. Draw curved arrows to show the movement of electrons in this step of the rxn mechanism. ci: CH2 : > cha
4. [12 pts] Propose mechanisms for the formation of all 3 products shown in the reaction below: (draw curved arrows, intermediates, and resonance structures if necessary. NO NEED FOR TRANSITION STATES! CH CH CH CH Br Heat CH,CH,OH OCH.CH Mechanism.14 points) Mechanism 2 points) Mechanism.3 14 points) 5. [14 pts] Provide the major products of reacting the alkene shown in the middle of the scheme below with all the reagents independently. Draw the products' structures in the corresponding table below...
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