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Acid-Catalyzed Aldol Condensation OH он steps 1. Provide curved arrows for each step (just the part...
Use curved arrows to indicate the flow of electrons for the following elementary steps. label each...
Use
curved arrows to indicate the flow of electrons for the following
elementary steps. label each step of the proper name such as Sn2,
E2, electrophile elimination, bond dissociation, coordination,
nucleophilic addition, electrophilic addition, or nucleophilic
elimination
These are the answers I had but they are incorrect... could
you explain which are correct?
4. Use curved arrow to indicate the flow of electrons for the following elementary steps. Label each-st with a proper name such as S 2, E2, electrophile...
OH H+ CH3 H3C OH Esters can be synthesized by an acid-catalyzed nucleophilic acyl substitution between...
OH H+ CH3 H3C OH Esters can be synthesized by an acid-catalyzed nucleophilic acyl substitution between an alcohol and a carboxylic acid; this process is called the Fischer esterification reaction. Because the alcohol oxygen is a poor nucleophile, the carbonyl carbon is made a better electrophile by protonation of the carbonyl oxygen. The steps of the synthesis are all reversible. The reaction is generally driven to completion by using an excess of the liquid alcohol as a solvent, or by...
3. Acids and Bases. (15 pts) (a) Circle the weakest acid in each series shown below (9 pts). Seri...
poease answer and explain all. thank you!
3. Acids and Bases. (15 pts) (a) Circle the weakest acid in each series shown below (9 pts). Series 1 HC CH2 Series 2 OH он OH Series 3 Cl ai pk, 9.38 pk, 10.2 (b) Draw the products of the following acid-base reaction (6 pts). CH3O reactants products 4. Use curved arrow to indieate the flow of electrons for the following elementary steps. Label each step with a proper name such as...
Question 1 Match each reagent with its role in aldol condensation reaction. Not yet answered D-anisaldehyde...
Question 1 Match each reagent with its role in aldol condensation reaction. Not yet answered D-anisaldehyde Choose... Points out of 10.00 dium hydroxide Choose... P Flag question acetophenone Choose... ethanol Choose... Question 2 Not yet answered To purify the aldol condensation product you will have to recrystallize it from methanol. Give the steps in recrystallization procedure the appropriate order numbering. Points out of 10.00 The compound is kept under vacuum for 10 min Choose... + P Flag question The solution...
1-24 need help really lost Proton Transfer: deprotonation D. 1) Add the appropriate curved arrows for...
1-24 need help really lost
Proton Transfer: deprotonation D. 1) Add the appropriate curved arrows for the following deprotonation step. Also add the other product notice how the Tema s can be converted to this by use of a strong base such as sodium a sodium ion (Na) is not drawn, in this case it is just a spectatorio PCW27 - Mechanistic steps - Part Name: Time spent 2) Label the above compounds with the appropriate name from the previous...
1. Below is a monosaccharide in its cyclic (ring) form. OH он Linear form OH a)...
1. Below is a monosaccharide in its cyclic (ring) form. OH он Linear form OH a) Is the monosaccharide the a-or the B-anomer? b) Label each carbon with its carbon number. c) Draw the linear form of this monosaccharide with the correct chirality in the box at right. 2. a) Draw the linear form of D-ribose: b) Ribose can form a pyranose ring. Draw an electron arrow on your linear ribose drawing above, indicating which nucleophile attacks which electrophile to...
Part A Use curved arrows to keep track of the electrons during the formation of an...
Part A Use curved arrows to keep track of the electrons during the formation of an enclate 3,3-dimethylbutan-2-one methode anion methanololate anion of 3,3-dimethylbutan-2-one Edit the reaction by drawing all steps in the appropriate boxes and connecting them with reaction arrows. Add charges where needed. Electron flow arrows should start on an om or a bond and should and on an atom, bond, or location where a new bond should be created DHO ISO 1 Part B The acid catalyzed...
1 pt 1 pt The final step in the hydration of an alkyne under acidic conditions...
1 pt 1 pt The final step in the hydration of an alkyne under acidic conditions is the automerization of an enol intermediate to give the corresponding ketone. The mechanism involves a protonation followed by deprotonation Consider the following tautomerization reaction: CH2 CHE H,09 1 pt 1 pt 1 pt OH 1 pt 1pl For the mechanism step below, draw curved arrows to show electron reorganization Where relevant, a pi bond has two hot spots when you draw a curved...
250 ChemActivity 29 Electrophilic Aromatic Substitution no ChemActivity 29 Part A: Electrophilic Aromatic Substitution (What products...
250 ChemActivity 29 Electrophilic Aromatic Substitution no ChemActivity 29 Part A: Electrophilic Aromatic Substitution (What products are formed when a strong electrophile is added to benzene?) Model 1: (review) Electrophilic Addition of HCI Rani o g cyclohexene carbocation intermediate Run 2 U X benzene This product carbocation intermediate DOES NOT Critical Thinking Questions 1 For Rxn I (above) draw curved arrows showing the mechanism of electrophilic addition of HCl. Include an appropriate carbocation intermediate in the box above. Figure 1:...
Use
curved arrows to indicate the flow of electrons for the following
elementary steps. label each step of the proper name such as Sn2,
E2, electrophile elimination, bond dissociation, coordination,
nucleophilic addition, electrophilic addition, or nucleophilic
elimination
These are the answers I had but they are incorrect... could
you explain which are correct?
4. Use curved arrow to indicate the flow of electrons for the following elementary steps. Label each-st with a proper name such as S 2, E2, electrophile...
OH H+ CH3 H3C OH Esters can be synthesized by an acid-catalyzed nucleophilic acyl substitution between an alcohol and a carboxylic acid; this process is called the Fischer esterification reaction. Because the alcohol oxygen is a poor nucleophile, the carbonyl carbon is made a better electrophile by protonation of the carbonyl oxygen. The steps of the synthesis are all reversible. The reaction is generally driven to completion by using an excess of the liquid alcohol as a solvent, or by...
poease answer and explain all. thank you!
3. Acids and Bases. (15 pts) (a) Circle the weakest acid in each series shown below (9 pts). Series 1 HC CH2 Series 2 OH он OH Series 3 Cl ai pk, 9.38 pk, 10.2 (b) Draw the products of the following acid-base reaction (6 pts). CH3O reactants products 4. Use curved arrow to indieate the flow of electrons for the following elementary steps. Label each step with a proper name such as...
Question 1 Match each reagent with its role in aldol condensation reaction. Not yet answered D-anisaldehyde Choose... Points out of 10.00 dium hydroxide Choose... P Flag question acetophenone Choose... ethanol Choose... Question 2 Not yet answered To purify the aldol condensation product you will have to recrystallize it from methanol. Give the steps in recrystallization procedure the appropriate order numbering. Points out of 10.00 The compound is kept under vacuum for 10 min Choose... + P Flag question The solution...
1-24 need help really lost
Proton Transfer: deprotonation D. 1) Add the appropriate curved arrows for the following deprotonation step. Also add the other product notice how the Tema s can be converted to this by use of a strong base such as sodium a sodium ion (Na) is not drawn, in this case it is just a spectatorio PCW27 - Mechanistic steps - Part Name: Time spent 2) Label the above compounds with the appropriate name from the previous...
1. Below is a monosaccharide in its cyclic (ring) form. OH он Linear form OH a) Is the monosaccharide the a-or the B-anomer? b) Label each carbon with its carbon number. c) Draw the linear form of this monosaccharide with the correct chirality in the box at right. 2. a) Draw the linear form of D-ribose: b) Ribose can form a pyranose ring. Draw an electron arrow on your linear ribose drawing above, indicating which nucleophile attacks which electrophile to...
Part A Use curved arrows to keep track of the electrons during the formation of an enclate 3,3-dimethylbutan-2-one methode anion methanololate anion of 3,3-dimethylbutan-2-one Edit the reaction by drawing all steps in the appropriate boxes and connecting them with reaction arrows. Add charges where needed. Electron flow arrows should start on an om or a bond and should and on an atom, bond, or location where a new bond should be created DHO ISO 1 Part B The acid catalyzed...
1 pt 1 pt The final step in the hydration of an alkyne under acidic conditions is the automerization of an enol intermediate to give the corresponding ketone. The mechanism involves a protonation followed by deprotonation Consider the following tautomerization reaction: CH2 CHE H,09 1 pt 1 pt 1 pt OH 1 pt 1pl For the mechanism step below, draw curved arrows to show electron reorganization Where relevant, a pi bond has two hot spots when you draw a curved...
250 ChemActivity 29 Electrophilic Aromatic Substitution no ChemActivity 29 Part A: Electrophilic Aromatic Substitution (What products are formed when a strong electrophile is added to benzene?) Model 1: (review) Electrophilic Addition of HCI Rani o g cyclohexene carbocation intermediate Run 2 U X benzene This product carbocation intermediate DOES NOT Critical Thinking Questions 1 For Rxn I (above) draw curved arrows showing the mechanism of electrophilic addition of HCl. Include an appropriate carbocation intermediate in the box above. Figure 1:...
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