Discoloration of p-phenetidine includes: 1) addition of HCl, 2) heating with activated carbon, and then 3)...
Discoloration of p-phenetidine includes: 1) addition of HCl, 2) heating with activated carbon, and then 3) addition of sodium acetate NaOCOCH3.
Write the equations behind the steps 1 and 3.
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Discoloration of p-phenetidine includes: 1) addition of HCl, 2)
heating with activated carbon, and then 3)...
The equilibrium of Co and CF with CoCl- 5 Initial Color: blue Color after addition of...
The equilibrium of Co and CF with CoCl- 5 Initial Color: blue Color after addition of HCI: Piuk bue/Paxle Color after addition of HCI: Color after heating: Pak Color after cooling: Questions Chatelier's Principle to explain the different colors found in the following equilibria. Write balance chemical equations for all chemical reactions. Write net ionic equations for the reaction between Fe(NO3)2(aq) and KSCN(aq) a Explain the color change when Fe(NO3)2 is added to the reaction at equilibrium. b Write net...
1. Complete the following addition reactions. Write balanced equations for each. • 2-butene with chlorine •...
1. Complete the following addition reactions. Write balanced equations for each. • 2-butene with chlorine • Ethene with hydrogen chloride (HCl)
Bonus 3. Give the structures of the two products for addition reaction of HCl to 3-methyl-1-pentene...
Bonus 3. Give the structures of the two products for addition reaction of HCl to 3-methyl-1-pentene (1 point). Point out which one is the major product, and explain why! (Hint: dont forget carbocation rearrangement) 4. The transformation of the alkyl chloride shown below into the alcohol can be accomplished in two steps. Show the synthetic scheme to finish the conversion. (1 point) Он Br
Write the equations that explain the following: 1 Kw 2 Ksp for HgS 3 Ka for...
Write the equations that explain the following: 1 Kw 2 Ksp for HgS 3 Ka for Formic acid (HCOOH) 4 Kd for Br2 5 Kb for sodium acetate 6 Kl for [Ni(CN)]+ 7 B4 for [pt(CN)4]2-
1. Hg(OAc)2, H20 2. NaBHA CH3 M HC CHE нас Acid-catalyzed addition of water to an...
1. Hg(OAc)2, H20 2. NaBHA CH3 M HC CHE нас Acid-catalyzed addition of water to an alkene yields an alcohol with Markovnikov regiochemistry. The electrophilic H adds to the sp carbon with the most hydrogens to yield the most stable carbocation intermediate, which then adds water to give the product alcohol. Because a carbocation intermediate is formed, rearrangements can occur prior to the addition of water To avoid the possibility of rearrangement and still give a Markovnikov alcohol, alkenes can...
Data Table 1. Mass of Beaker 49.93g 2. Mass of beaker + Na2CO3 50.95g 3....
Data Table 1. Mass of Beaker 49.93g 2. Mass of beaker + Na2CO3 50.95g 3. Mass of Na2CO3 added into the beaker (line 2-line 1) 1.02g 4. Mass of graduated cylinder with 3M HCl solution 12.68g 5. Mass of graduated cylinder without 3M HCl solution 4.44g 6. Mass of 3M HCL solution added into the beaker (line4-line5) 8.24g 7. Mass of beaker + reactants (HCl+ Na2CO3; line 2+line 6) 59.19g 8. Mass of beaker + products without CO2 (after...
CH3 CH3 1. Hg(OAC), H20 2. NaBH НО, І CH3 CH, Hoc H₃C/ Acid-catalyzed addition of...
CH3 CH3 1. Hg(OAC), H20 2. NaBH НО, І CH3 CH, Hoc H₃C/ Acid-catalyzed addition of water to an alkene yields an alcohol with Markovnikov regiochemistry. The electrophilic H adds to the sp carbon with the most hydrogens to yield the most stable carbocation intermediate, which then adds water to give the product alcohol. Because a carbocation intermediate is formed, rearrangements can occur prior to the addition of water. To avoid the possibility of rearrangement and still give a Markovnikov...
2 problems 1. Hg(OAC)2, H20 2. NaBHg CH3 H3C H₃C Acid-catalyzed addition of water to an...
2
problems
1. Hg(OAC)2, H20 2. NaBHg CH3 H3C H₃C Acid-catalyzed addition of water to an alkene yields an alcohol with Markovnikov regiochemistry. The electrophilic add carbon with the most hydrogens to yield the most stable carbocation intermediate, which then adds water to give the produc Because a carbocation intermediate is formed, rearrangements can occur prior to the addition of water. To avoid the possibility of rearrangement and still give a Markovnikov alcohol, alkenes can instead be treated with mercury...
a) Which products (shown above) from reaction 3 can react with HCl in an acid-base reaction?...
a) Which products (shown above) from reaction 3 can react with
HCl in an acid-base reaction? Show the mechanism for this acid-base
reaction and give the structures that would result from the
protonation of these products. Which phase (organic or aqueous)
would these protonated products be soluble in?
b) Which phase (organic or aqueous) would the
p-methylacetanilide be found in?
In step 5 of reaction 3, the reaction mixture containing the products shown below in ethyl acetate is extracted twice...
1. Write a structural formula for each of the following compounds: (36 pts) (a) m-chlorobenzoyl chloride...
1. Write a structural formula for each of the following compounds: (36 pts) (a) m-chlorobenzoyl chloride (b) N-ethyl benzamide (c) dibenzalacetone (d) ethyl acetoacetate (e) 2-ethyl-1-butanamine (t) dibenzylamine 2. Write a structural formula for the principal organic product or products of each of the following reactions: (36 pts) (a) propanoyl chloride and sodium propanoate (b) acetic anhydride and 3-pentanol (c) acetaldehyde and sodium ethoxide (CH3CH2ONa) in ethanol solvent (d) cyclohexanone, benzaldehyde, and NaOH (e) 2-aminopropane and acetyl chloride in pyridine...
The equilibrium of Co and CF with CoCl- 5 Initial Color: blue Color after addition of HCI: Piuk bue/Paxle Color after addition of HCI: Color after heating: Pak Color after cooling: Questions Chatelier's Principle to explain the different colors found in the following equilibria. Write balance chemical equations for all chemical reactions. Write net ionic equations for the reaction between Fe(NO3)2(aq) and KSCN(aq) a Explain the color change when Fe(NO3)2 is added to the reaction at equilibrium. b Write net...
Bonus 3. Give the structures of the two products for addition reaction of HCl to 3-methyl-1-pentene (1 point). Point out which one is the major product, and explain why! (Hint: dont forget carbocation rearrangement) 4. The transformation of the alkyl chloride shown below into the alcohol can be accomplished in two steps. Show the synthetic scheme to finish the conversion. (1 point) Он Br
1. Hg(OAc)2, H20 2. NaBHA CH3 M HC CHE нас Acid-catalyzed addition of water to an alkene yields an alcohol with Markovnikov regiochemistry. The electrophilic H adds to the sp carbon with the most hydrogens to yield the most stable carbocation intermediate, which then adds water to give the product alcohol. Because a carbocation intermediate is formed, rearrangements can occur prior to the addition of water To avoid the possibility of rearrangement and still give a Markovnikov alcohol, alkenes can...
CH3 CH3 1. Hg(OAC), H20 2. NaBH НО, І CH3 CH, Hoc H₃C/ Acid-catalyzed addition of water to an alkene yields an alcohol with Markovnikov regiochemistry. The electrophilic H adds to the sp carbon with the most hydrogens to yield the most stable carbocation intermediate, which then adds water to give the product alcohol. Because a carbocation intermediate is formed, rearrangements can occur prior to the addition of water. To avoid the possibility of rearrangement and still give a Markovnikov...
2
problems
1. Hg(OAC)2, H20 2. NaBHg CH3 H3C H₃C Acid-catalyzed addition of water to an alkene yields an alcohol with Markovnikov regiochemistry. The electrophilic add carbon with the most hydrogens to yield the most stable carbocation intermediate, which then adds water to give the produc Because a carbocation intermediate is formed, rearrangements can occur prior to the addition of water. To avoid the possibility of rearrangement and still give a Markovnikov alcohol, alkenes can instead be treated with mercury...
a) Which products (shown above) from reaction 3 can react with
HCl in an acid-base reaction? Show the mechanism for this acid-base
reaction and give the structures that would result from the
protonation of these products. Which phase (organic or aqueous)
would these protonated products be soluble in?
b) Which phase (organic or aqueous) would the
p-methylacetanilide be found in?
In step 5 of reaction 3, the reaction mixture containing the products shown below in ethyl acetate is extracted twice...
1. Write a structural formula for each of the following compounds: (36 pts) (a) m-chlorobenzoyl chloride (b) N-ethyl benzamide (c) dibenzalacetone (d) ethyl acetoacetate (e) 2-ethyl-1-butanamine (t) dibenzylamine 2. Write a structural formula for the principal organic product or products of each of the following reactions: (36 pts) (a) propanoyl chloride and sodium propanoate (b) acetic anhydride and 3-pentanol (c) acetaldehyde and sodium ethoxide (CH3CH2ONa) in ethanol solvent (d) cyclohexanone, benzaldehyde, and NaOH (e) 2-aminopropane and acetyl chloride in pyridine...
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