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sergij07 [2.7K]
3 years ago
7

In a robinson annulation, an α,-unsaturated carbonyl compound reacts with a carbonyl compound to afford a (new) cyclic α,-unsa

turated ketone by a michael–aldol–dehydration sequence. draw the structure of the reactants that would combine to form the a ring of the steroid desoxy-19-nortestosterone (below) by a robinson annulation.

Chemistry
1 answer:
Marina CMI [18]3 years ago
4 0
Robinson Annulation reaction is mainly done for the synthesis of six membered rings. This reaction is the combination of two reactions 1). Michael Addition Reaction and 2). Aldole Condensation.

The synthesis of <span>desoxy-19-nortestosterone by Robinson Annulation is shown below,</span>

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Answer:

Option 3. The catalyst does not affect the enthalpy change (\Delta H_\text{rxn}) of a reaction.

Explanation:

As its name suggests, the enthalpy change of a reaction (\Delta H_\text{rxn}) is the difference between the enthalpy of the products and the reactants.

On the other hand, a catalyst speeds up a reaction because it provides an alternative reaction pathway from the reactants to the products.

In effect, a catalyst reduces the activation energy of the reaction in both directions. The reactants and products of the reaction won't change. As a result, the difference in their enthalpies won't change, either. That's the same as saying that the enthalpy change \Delta H_\text{rxn} of the reaction would stay the same.

Refer to an energy profile diagram. Enthalpy change of the reaction \Delta H_\text{rxn} measures the difference between the two horizontal sections. Indeed, the catalyst lowered the height of the peak. However, that did not change the height of each horizontal section or the difference between them. Hence, the enthalpy change of the reaction stayed the same.

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Identify the family to which the compound (h3c−ch2oh) belongs. identify the family to which the compound (a) belongs. alcohol et
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4 0
3 years ago
Calculate the pH for each of the following cases in the titration of 50.0 mL of 0.210 M HClO(aq) with 0.210 M KOH(aq).
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a) before addition of any KOH : 

when we use the Ka equation & Ka = 4 x 10^-8 : 

Ka = [H+]^2 / [ HCIO]

by substitution:

4 x 10^-8 = [H+]^2 / 0.21

[H+]^2 = (4 x 10^-8) * 0.21

           = 8.4 x 10^-9

[H+] = √(8.4 x 10^-9)

       = 9.2 x 10^-5 M

when PH = -㏒[H+]

   PH = -㏒(9.2 x 10^-5)

        = 4  

b)After addition of 25 mL of KOH: this produces a buffer solution 

So, we will use Henderson-Hasselbalch equation to get PH:

PH = Pka +㏒[Salt]/[acid]


first, we have to get moles of HCIO= molarity * volume

                                                           =0.21M * 0.05L

                                                           = 0.0105 moles

then, moles of KOH = molarity * volume 

                                  = 0.21 * 0.025

                                  =0.00525 moles 

∴moles HCIO remaining = 0.0105 - 0.00525 = 0.00525

and when the total volume is = 0.05 L + 0.025 L =  0.075 L

So the molarity of HCIO = moles HCIO remaining / total volume

                                        = 0.00525 / 0.075

                                        =0.07 M

and molarity of KCIO = moles KCIO / total volume

                                    = 0.00525 / 0.075

                                    = 0.07 M

and when Ka = 4 x 10^-8 

∴Pka =-㏒Ka

         = -㏒(4 x 10^-8)

         = 7.4 

by substitution in H-H equation:

PH = 7.4 + ㏒(0.07/0.07)

∴PH = 7.4 

c) after addition of 35 mL of KOH:

we will use the H-H equation again as we have a buffer solution:

PH = Pka + ㏒[salt/acid]

first, we have to get moles HCIO = molarity * volume 

                                                        = 0.21 M * 0.05L

                                                        = 0.0105 moles

then moles KOH = molarity * volume
                            =  0.22 M* 0.035 L 

                            =0.0077 moles 

∴ moles of HCIO remaining = 0.0105 - 0.0077=  8 x 10^-5

when the total volume = 0.05L + 0.035L = 0.085 L

∴ the molarity of HCIO = moles HCIO remaining / total volume 

                                      = 8 x 10^-5 / 0.085

                                      = 9.4 x 10^-4 M

and the molarity of KCIO = moles KCIO / total volume

                                          = 0.0077M / 0.085L

                                          = 0.09 M

by substitution:

PH = 7.4 + ㏒( 0.09 /9.4 x 10^-4)

∴PH = 8.38

D)After addition of 50 mL:

from the above solutions, we can see that 0.0105 mol HCIO reacting with 0.0105 mol KOH to produce 0.0105 mol KCIO which dissolve in 0.1 L (0.5L+0.5L) of the solution.

the molarity of KCIO = moles KCIO / total volume

                                   = 0.0105mol / 0.1 L

                                   = 0.105 M

when Ka = KW / Kb

∴Kb = 1 x 10^-14 / 4 x 10^-8

       = 2.5 x 10^-7

by using Kb expression:

Kb = [CIO-] [OH-] / [KCIO]

when [CIO-] =[OH-] so we can substitute by [OH-] instead of [CIO-]

Kb = [OH-]^2 / [KCIO] 

2.5 x 10^-7 = [OH-]^2 /0.105

∴[OH-] = 0.00016 M

POH = -㏒[OH-]

∴POH = -㏒0.00016

           = 3.8
∴PH = 14- POH

        =14 - 3.8

PH = 10.2

e) after addition 60 mL of KOH:

when KOH neutralized all the HCIO so, to get the molarity of KOH solution

M1*V1= M2*V2

 when M1 is the molarity of KOH solution

V1 is the total volume = 0.05 + 0.06 = 0.11 L

M2 = 0.21 M 

V2 is the excess volume added  of KOH = 0.01L

so by substitution:

M1 * 0.11L = 0.21*0.01L

∴M1 =0.02 M

∴[KOH] = [OH-] = 0.02 M

∴POH = -㏒[OH-]

           = -㏒0.02 

           = 1.7

∴PH = 14- POH

       = 14- 1.7 

      = 12.3 
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3 years ago
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