Can someone explain the mechanisms + products for these reactions?
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Can someone explain the mechanisms + products for these
reactions?
1. (3p) Draw the mechanism and...
1. (3p) Draw the mechanism and the expected reaction product for the following reaction: 2. (3p)...
1. (3p) Draw the mechanism and the expected reaction product for the following reaction: 2. (3p) Draw the mechanism and the expected Nucleophilic Substitution Reaction Product for the following reaction: OH 3. (3p) What reagent is necessary in the hydrolysis of carboxylic acid derivatives? Rank these derivatives in order of their reactivity.
1. (3p) Draw the mechanism and the expected reaction product for the following reaction: xo 2....
1. (3p) Draw the mechanism and the expected reaction product for the following reaction: xo 2. (3p) Draw the mechanism and the expected Nucleophilic Substitution Reaction Product for the following reaction: 3. (3p) What reagent is necessary in the hydrolysis of carboxylic acid derivatives? Rank these derivatives in order of their reactivity. 4. (3p) Write the product for the following reaction: NaOH CHO 5. (3p) Propose a synthesis for the following compound by using a Witting reaction:
Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed....
Identify the mechanism by which each of the
reactions above proceeds from among the mechanisms listed. Use the
letters a - i for your
answers.
1. HC (Ph)3C-OH (Ph)3C-C + H.о 2. Нао он + conc. HC g SNl Nucleophilic substitution d Electrophilic addition a Proton transfer h SN2 Nucleophilic substitution e E1 Elimination b Lewis acid/base Radical chain substitution f E2 Elimination Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use...
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...
Can someone please predict the major products and PLEASE put the mechanisms so I know how...
Can someone please predict the major products and PLEASE put the
mechanisms so I know how the products were obtained and for #3 the
IUPAC name.
Problem #1 Draw the major product(s) expected from the following sequence of reactions: 1. I-BOK 2. Og 3. DMS Problem #2 Complete the following reactions: H (9) CHE Na', NH3(0) H3C H2(g) Pd on Caco, Pbо, Problem #3 Provide the full IUPAC name for the following molecule. H3C Нас Problem #4 Draw the substitution...
1. Determine the mechanism of each nucleophilic substitution reaction and explain why? Draw the products including...
1. Determine the mechanism of each nucleophilic substitution reaction and explain why? Draw the products including the stereochemistry. (6 points) Br + CN acetone d. ~ + CH,CO2H - Y Y + POCHE UCH DMSO + TOCH.CH DMF b. + B + OCH + CH4OH DMSO – w ! ho + OCHCH , CH,CH,OH DM . Br + CH3OH + CH3CH,OH
Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed....
Identify the mechanism by which each of the reactions above
proceeds from among the mechanisms listed. Use the letters
a - i for your answers.
Methanol to + + NaOCH3 NOCH Mothands t º + HOCH • NAGI HOCHZ + NaCl OH NaHCO3 o + H2O + CO2 + Nal a = Proton transfer b = Lewis acid base c = Radical chain substitution d=Radical chain addition e = Electrophilic addition f=E1 Elimination g=E2 Elimination h=Syl Nucleophilic substitution i= Sy2...
Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed....
Identify the mechanism by
which each of the reactions above proceeds from among the
mechanisms listed. Use the letters a - j for your answers.
OH 1. +HI hv N-Br N-H CCl a-Proton transfer b = Lewis acid base c Radical chain substitution d - Radical chain addition e Electrophilic addition fEl Elimination g E2 Elimination h- SN1 Nucleophilic substitutiorn i - SN2 Nucleophilic substitution J -Electrophilic aromatic substituticn Identify the mechanism by which each of the reactions above proceeds...
Draw the products for these reactions. In cases where more than one product is formed, identify...
Draw the products for these reactions. In cases where more than
one product is formed, identify the major product. Also, in cases
where a nucleophilic substitution occurs, identify the mechanism to
be either SN1 or SN2
NaBH CH3 OH H3C
Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed....
Identify the mechanism by which each of the reactions above
proceeds from among the mechanisms listed. Use the letters
a - i for your answers.
HCI NH2 NH sobe. The ZI a= Proton transfer d=Sn2 Nucleophilic substitution e= Electrophilic aromatic substitution f= Carbonyl nucleophilic addn g= Nucleophilic subs at carbonyl(acyl Xfer) h = Conjugate (nucleophilic) addn b = Lewis acid/base c=E2 elimination Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the...
1. (3p) Draw the mechanism and the expected reaction product for the following reaction: 2. (3p) Draw the mechanism and the expected Nucleophilic Substitution Reaction Product for the following reaction: OH 3. (3p) What reagent is necessary in the hydrolysis of carboxylic acid derivatives? Rank these derivatives in order of their reactivity.
1. (3p) Draw the mechanism and the expected reaction product for the following reaction: xo 2. (3p) Draw the mechanism and the expected Nucleophilic Substitution Reaction Product for the following reaction: 3. (3p) What reagent is necessary in the hydrolysis of carboxylic acid derivatives? Rank these derivatives in order of their reactivity. 4. (3p) Write the product for the following reaction: NaOH CHO 5. (3p) Propose a synthesis for the following compound by using a Witting reaction:
Identify the mechanism by which each of the
reactions above proceeds from among the mechanisms listed. Use the
letters a - i for your
answers.
1. HC (Ph)3C-OH (Ph)3C-C + H.о 2. Нао он + conc. HC g SNl Nucleophilic substitution d Electrophilic addition a Proton transfer h SN2 Nucleophilic substitution e E1 Elimination b Lewis acid/base Radical chain substitution f E2 Elimination Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use...
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...
Can someone please predict the major products and PLEASE put the
mechanisms so I know how the products were obtained and for #3 the
IUPAC name.
Problem #1 Draw the major product(s) expected from the following sequence of reactions: 1. I-BOK 2. Og 3. DMS Problem #2 Complete the following reactions: H (9) CHE Na', NH3(0) H3C H2(g) Pd on Caco, Pbо, Problem #3 Provide the full IUPAC name for the following molecule. H3C Нас Problem #4 Draw the substitution...
1. Determine the mechanism of each nucleophilic substitution reaction and explain why? Draw the products including the stereochemistry. (6 points) Br + CN acetone d. ~ + CH,CO2H - Y Y + POCHE UCH DMSO + TOCH.CH DMF b. + B + OCH + CH4OH DMSO – w ! ho + OCHCH , CH,CH,OH DM . Br + CH3OH + CH3CH,OH
Identify the mechanism by which each of the reactions above
proceeds from among the mechanisms listed. Use the letters
a - i for your answers.
Methanol to + + NaOCH3 NOCH Mothands t º + HOCH • NAGI HOCHZ + NaCl OH NaHCO3 o + H2O + CO2 + Nal a = Proton transfer b = Lewis acid base c = Radical chain substitution d=Radical chain addition e = Electrophilic addition f=E1 Elimination g=E2 Elimination h=Syl Nucleophilic substitution i= Sy2...
Identify the mechanism by
which each of the reactions above proceeds from among the
mechanisms listed. Use the letters a - j for your answers.
OH 1. +HI hv N-Br N-H CCl a-Proton transfer b = Lewis acid base c Radical chain substitution d - Radical chain addition e Electrophilic addition fEl Elimination g E2 Elimination h- SN1 Nucleophilic substitutiorn i - SN2 Nucleophilic substitution J -Electrophilic aromatic substituticn Identify the mechanism by which each of the reactions above proceeds...
Draw the products for these reactions. In cases where more than
one product is formed, identify the major product. Also, in cases
where a nucleophilic substitution occurs, identify the mechanism to
be either SN1 or SN2
NaBH CH3 OH H3C
Identify the mechanism by which each of the reactions above
proceeds from among the mechanisms listed. Use the letters
a - i for your answers.
HCI NH2 NH sobe. The ZI a= Proton transfer d=Sn2 Nucleophilic substitution e= Electrophilic aromatic substitution f= Carbonyl nucleophilic addn g= Nucleophilic subs at carbonyl(acyl Xfer) h = Conjugate (nucleophilic) addn b = Lewis acid/base c=E2 elimination Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the...
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