I need help on number 1 and for number 2 how would I draw the
energy diagram? Also, is number 3 correct? Thanks in advance!Homework Answers
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I need help on number 1 and for number 2 how would I draw the
energy...
I need help on all of these please 1. Draw the energy diagram that correctly depicts...
I need help on all of these please
1. Draw the energy diagram that correctly depicts the following reaction (AG<0) and the transition state for the rate determining step. Label substrate (S), product (P), and intermediate (1) if applicable. OTS + NaBr TsONa polar aprotic solvent transition state free energy reaction progress 2. Complete the following reaction schemes. CH3OH 0°C alkyl halide nucleophile ТА polar aprotic solvent 3. Compound A and B are constitutional isomers with molecular formula C5H11Br. When...
Help please!! With the number of the questions and everything legible :) 1. Name compounds below...
Help please!!
With the number of the questions and everything legible
:)
1. Name compounds below according to the IUPAC nomenclature (1 point each) 2E4Syheant-bromo 2- hep tene 2 methy1-abexene , , 3 ?,-trimethyl-cyclone-ene 2, Determine which alkenes will roduce 3-methylpentane in the process of catalytic hydrogenation and write chemica equations of these reactions (5 points) C H 13-mem-2-p enters Write the dehydration reaction, draw and name all possible products, select the major product and explain why (Ss pints): what...
I need help on all of these. Any help is much appreciated! 3. The enzyme aconitase...
I
need help on all of these. Any help is much appreciated!
3. The enzyme aconitase catalyzes the hydration (addition of water across the double bond) of aconitic acid to two products: citric acid and isocitric acid. Isocitric acid is optically active, citric acid is not. What are the structures of citric acid and isocitric acid? но HO Aconitic Acid 4. Compound A has the molecular formula of C:Hı2 and reacts with 2 equivalents of H2. A gives HCOCH2CH2CHO as...
please draw energy diagram with answer 1) The compound below does not undergo an S 2...
please draw energy diagram with answer
1) The compound below does not undergo an S 2 reaction despite being a primary alkyl chloride. Draw the arrow pushing mechanism for an S 2 reaction if one did occur; then use a reaction energy diagram to explain why the S 2 reaction does not occur. (10 points) XcNaSH N. R.
6) Draw the structure of (Z)-1-chloro-2-methyl-2-butene. 7) Draw the curved arrows to show how CH3CH=CHCH2CH3 reacts...
6) Draw the structure of (Z)-1-chloro-2-methyl-2-butene. 7) Draw the curved arrows to show how CH3CH=CHCH2CH3 reacts with HBr to form a carbocation first, and then forms 2-bromopentane. (this is 2 steps) 7) 8) 8) Predict the product(s) of the following reaction based on the curved arrows: Make sure to include + and- charges where appropriate. -C-NH2 CH CHy HO 9) Based on the following reaction coordinate diagram: Which compound, A or C, is formed faster from B? Which is more...
can you please draw the number or e- (1 or 2) with the arrows instead of...
can you please draw the number or e- (1 or 2) with the arrows
instead of arrows?
Reaction of 3-methyl-1-butene with CH2OH in the presence of H2SO4 catalyst yields 2-methoxy-2-methylbutane by a mechanism analogous to that of acid- catalyzed alkene hydration. Draw curved arrows to show the movement of electrons in this step of the reaction mechanism. Arrow-pushing Instructions носн y CH3OH amen - Submit Answer Try Another Version 2 item attempts remaining CO2CH3 CO2CH3 Hg(OAC)2 AcOHg Draw curved arrows...
(a) Draw the saw-horse (or wedge-dash) projection of (2S,3R)-3-methylpentan-2-ol. [Marks: 1] (b) Draw the Newman projections...
(a) Draw the saw-horse (or wedge-dash) projection of (2S,3R)-3-methylpentan-2-ol. [Marks: 1] (b) Draw the Newman projections of the 2-3 bond in (2S,3R)-3-methylpentan-2-ol. [Marks: 2] (c) Based on the Newman projections from part b. - draw a rotation vs. energy diagram (you do NOT need to give specific energy values in this diagram) that will allow you to identify the most stable confirmation around the 2-3 bond. Assume the greatest steric and torsional strain occurs when the hydroxyl and ethyl groups...
I need help with number 1 and 2 how to calculate the energy needs and based...
I need help with number 1 and 2 how to calculate the energy
needs and based on what factors?
This is for Nutrition subject
Thank you
Yow Peieve an DoSee Datient enine pPope Pecommendation. andl the feelim and r ohe month due tr 匕Dx. Chrnic Pancreatitis , Hx:aleha/ abuse 0 d Die A mylase ast tutorn Asess weidht measurements and uht t tels y ado.tm attent's natríkon ctat How? Lstincte en erayneeds, fluid needs heeds for this petient
please help The dehydration of alcohols Under acidic conditions, alcohols will undergo a dehydration reaction, producing...
please help
The dehydration of alcohols Under acidic conditions, alcohols will undergo a dehydration reaction, producing an alkene and water. During the reaction, the hydroxyl group of the alcohol and a hydrogen atom from an adjacent carbon atom are lost. The reaction takes place in three steps, as shown in the diagram. (Figure 1) In the first step, a hydrogen lon bonds to the hydroxyl group of the alcohol. In the second step, the protonated hydroxl group leaves the compound,...
I need help with number 1 and 2. Good Average s drawn 0% 2) bond. The...
I need help with number 1 and 2.
Good Average s drawn 0% 2) bond. The fist for the molecule. The second should be the LEAST stable (highest energy) Newman projection. Most Stable highest Least Stable CH3
I need help on all of these please
1. Draw the energy diagram that correctly depicts the following reaction (AG<0) and the transition state for the rate determining step. Label substrate (S), product (P), and intermediate (1) if applicable. OTS + NaBr TsONa polar aprotic solvent transition state free energy reaction progress 2. Complete the following reaction schemes. CH3OH 0°C alkyl halide nucleophile ТА polar aprotic solvent 3. Compound A and B are constitutional isomers with molecular formula C5H11Br. When...
Help please!!
With the number of the questions and everything legible
:)
1. Name compounds below according to the IUPAC nomenclature (1 point each) 2E4Syheant-bromo 2- hep tene 2 methy1-abexene , , 3 ?,-trimethyl-cyclone-ene 2, Determine which alkenes will roduce 3-methylpentane in the process of catalytic hydrogenation and write chemica equations of these reactions (5 points) C H 13-mem-2-p enters Write the dehydration reaction, draw and name all possible products, select the major product and explain why (Ss pints): what...
I
need help on all of these. Any help is much appreciated!
3. The enzyme aconitase catalyzes the hydration (addition of water across the double bond) of aconitic acid to two products: citric acid and isocitric acid. Isocitric acid is optically active, citric acid is not. What are the structures of citric acid and isocitric acid? но HO Aconitic Acid 4. Compound A has the molecular formula of C:Hı2 and reacts with 2 equivalents of H2. A gives HCOCH2CH2CHO as...
please draw energy diagram with answer
1) The compound below does not undergo an S 2 reaction despite being a primary alkyl chloride. Draw the arrow pushing mechanism for an S 2 reaction if one did occur; then use a reaction energy diagram to explain why the S 2 reaction does not occur. (10 points) XcNaSH N. R.
6) Draw the structure of (Z)-1-chloro-2-methyl-2-butene. 7) Draw the curved arrows to show how CH3CH=CHCH2CH3 reacts with HBr to form a carbocation first, and then forms 2-bromopentane. (this is 2 steps) 7) 8) 8) Predict the product(s) of the following reaction based on the curved arrows: Make sure to include + and- charges where appropriate. -C-NH2 CH CHy HO 9) Based on the following reaction coordinate diagram: Which compound, A or C, is formed faster from B? Which is more...
can you please draw the number or e- (1 or 2) with the arrows
instead of arrows?
Reaction of 3-methyl-1-butene with CH2OH in the presence of H2SO4 catalyst yields 2-methoxy-2-methylbutane by a mechanism analogous to that of acid- catalyzed alkene hydration. Draw curved arrows to show the movement of electrons in this step of the reaction mechanism. Arrow-pushing Instructions носн y CH3OH amen - Submit Answer Try Another Version 2 item attempts remaining CO2CH3 CO2CH3 Hg(OAC)2 AcOHg Draw curved arrows...
(a) Draw the saw-horse (or wedge-dash) projection of (2S,3R)-3-methylpentan-2-ol. [Marks: 1] (b) Draw the Newman projections of the 2-3 bond in (2S,3R)-3-methylpentan-2-ol. [Marks: 2] (c) Based on the Newman projections from part b. - draw a rotation vs. energy diagram (you do NOT need to give specific energy values in this diagram) that will allow you to identify the most stable confirmation around the 2-3 bond. Assume the greatest steric and torsional strain occurs when the hydroxyl and ethyl groups...
I need help with number 1 and 2 how to calculate the energy
needs and based on what factors?
This is for Nutrition subject
Thank you
Yow Peieve an DoSee Datient enine pPope Pecommendation. andl the feelim and r ohe month due tr 匕Dx. Chrnic Pancreatitis , Hx:aleha/ abuse 0 d Die A mylase ast tutorn Asess weidht measurements and uht t tels y ado.tm attent's natríkon ctat How? Lstincte en erayneeds, fluid needs heeds for this petient
please help
The dehydration of alcohols Under acidic conditions, alcohols will undergo a dehydration reaction, producing an alkene and water. During the reaction, the hydroxyl group of the alcohol and a hydrogen atom from an adjacent carbon atom are lost. The reaction takes place in three steps, as shown in the diagram. (Figure 1) In the first step, a hydrogen lon bonds to the hydroxyl group of the alcohol. In the second step, the protonated hydroxl group leaves the compound,...
I need help with number 1 and 2.
Good Average s drawn 0% 2) bond. The fist for the molecule. The second should be the LEAST stable (highest energy) Newman projection. Most Stable highest Least Stable CH3
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