NO3-(aq) + 2H+(aq) + e- --- NO2(g) + H2O(l) Ered = +0.80 VCu(s) -.pdf

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NO3-(aq) + 2H+(aq) + e- ---> NO2(g) + H2O(l) Ered = +0.80 V Cu(s) ---> Cu2+(aq) + 2e- Eox = -0.34 v Ecell = Eox + Ered = 0.80 - 0.34 = + 0.46 V Solution NO3-(aq) + 2H+(aq) + e- ---> NO2(g) + H2O(l) Ered = +0.80 V Cu(s) ---> Cu2+(aq) + 2e- Eox = -0.34 v Ecell = Eox + Ered = 0.80 - 0.34 = + 0.46 V.

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RNs role in kidney transplant recipient in the immediate post-operative period; RN\'s role in organ transplantation to assess, plan, implement, practice evidence based approach to evaluate care interventions in the care of the transplant patient . To analyse the biological, psychological and sociological effects of transplantation on the patient. Post-transplant nursing care for the patient begins in the post-anesthesia care unit. The first 24 hours after transplantation represent a critical period, marked by hemodynamic and respiratory instability, and there is a great risk of developing complications, mainly of graft rejection. The nurse treating the patient in the early post-transplant period needs specialized knowledge to reduce the problems, prevent or anticipate and intervene immediately to maximize the result of long-term graft and provide quality care throughout the hospitalization period. The behavior of diuresis is the most important element in the monitoring of renal functions, since it causes therapeutic behaviors such as hydration, medication and even surgery for urologic complications. The urinary catheter placement provides accurate measurement of urine output and determines the presence of hemorrhage and blood clot, acute graft rejection, and vascular thrombosis, and is a predictor of the development of transplantation. The urinary catheter is removed after proper healing of the anastomosis of the ureter into the bladder, when continued monitoring of urine volume is required. During the hospitalization of the patient, daily blood tests must be done, with the most relevant results including levels of serum creatinine, polymerase chain reaction (PCR), white cell count, and levels of immunosuppressive drugs. These parameters determine that the kidney function is effective and show the first signs of a possible rejection or infection, and whether the drug levels are within the therapeutic range required for the maintenance of immunosuppression or induction, maintenance and treatment of rejection. The nurse should moniter the patient\'s hemodynamic status and fluid volume to avoid post- transplant complications while maintaining central venous pressure at 10 mmHg and systolic blood pressure above 120 mmHg. Urine output is replaced on an hourly milliliter-for-milliliter basis and should be recorded hourly. RNs role in kidney transplant donor in the immediate post-operative period Donors face the possibility of post-operative complications such as bleeding, wound infection, fever, etc. Most of the post-operative complications are generally short-term and can be addressed with quality medical care. Closely monitor the renal function to assess for impairment and monitor the hematocrit to asses for bleeding . Donors experience more pain than recipient. Donor who had an open surgical approach may experience more pain than when a laproscopic approach used. Donors who had open approach will be usually discharged from hospital in 4 or 5 day.

RNs role in kidney transplant recipient in the immediate post-operat.pdf

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Corporate form of business is where an entity is owned by a small or large group of people ,called owners /shareholders ,each of whose liability is limited by shares--subject to laws of the state in which it operates. It has access to finance through issue of shares in the public It is a separate legal entity ,distinct from its shareholders.So, unlike ,sole-proprietorships& partnerships, the shareholders are not personally liable,if the business goes into liquidation. But,the primary disadvantage of this type of business form is double taxation of earnings & dividends of the company. ie. Any distribution of profits to shareholders ,is only from after- tax(corporate tax rate) income of the company. But they are also taxed at the personal level,on receipt of dividends,at the hands of the shareholders.So, the shareholder is subject to double taxation . So, ANSWER: b) double taxation Solution Corporate form of business is where an entity is owned by a small or large group of people ,called owners /shareholders ,each of whose liability is limited by shares--subject to laws of the state in which it operates. It has access to finance through issue of shares in the public It is a separate legal entity ,distinct from its shareholders.So, unlike ,sole-proprietorships& partnerships, the shareholders are not personally liable,if the business goes into liquidation. But,the primary disadvantage of this type of business form is double taxation of earnings & dividends of the company. ie. Any distribution of profits to shareholders ,is only from after- tax(corporate tax rate) income of the company. But they are also taxed at the personal level,on receipt of dividends,at the hands of the shareholders.So, the shareholder is subject to double taxation . So, ANSWER: b) double taxation.

Corporate form of business is where an entity is owned by a small .pdf

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Well first thing to remember is that C,N,S, and P are more often the central atom because they are more likely to bond with more atoms than O,F,H, and Cl. If it wants to bond with more atoms naturally, it will be at the center more often. (If a C always wants 4 atoms attached to it, it will usually get 4 atoms to attach to it, making it the center). Well choice a. can be thrown out because its saying that C,N,S, and P cannot hybridize atomic orbitals (which is already wrong) to allow as many bonds as allowed (meaning that because they can\'t hybridize, they cant hold as many bonds). This is an argument against why they are not central atoms. Choice d. can be thrown out too as well because O,F,H, and Cl are less metalic than the others, yet they do not take as many electrons (because the more electrons an atom shares, the more bonds it makes). If this was true, O,F,H, and Cl would act more as central atoms. This is also a negative argument. Left is B and C. C states that more metallic nonmetals have more desire for electrons, meaning C,N,S, and P want more electrons. This seems true, but then why does B usually only become BF3, meaning they do not want more electrons. B is true because it says that O,F,H, and Cl are less likely to share electrons with more than 2 atoms. It doesn\'t say why, just that it is less likely to. This is true because the sharing electrons with an atom = forming a bond with an atom. So if they don\'t want to share electrons with more than 2, it means they don\'t want to naturally form bonds with more than 2 atoms, which is absolutely true. Compared to C,N,S, and P who are more likely to share electrons with more than 2 atoms and bonding with more atoms meaning they are more often bonded to several atoms aka being the center. Solution Well first thing to remember is that C,N,S, and P are more often the central atom because they are more likely to bond with more atoms than O,F,H, and Cl. If it wants to bond with more atoms naturally, it will be at the center more often. (If a C always wants 4 atoms attached to it, it will usually get 4 atoms to attach to it, making it the center). Well choice a. can be thrown out because its saying that C,N,S, and P cannot hybridize atomic orbitals (which is already wrong) to allow as many bonds as allowed (meaning that because they can\'t hybridize, they cant hold as many bonds). This is an argument against why they are not central atoms. Choice d. can be thrown out too as well because O,F,H, and Cl are less metalic than the others, yet they do not take as many electrons (because the more electrons an atom shares, the more bonds it makes). If this was true, O,F,H, and Cl would act more as central atoms. This is also a negative argument. Left is B and C. C states that more metallic nonmetals have more desire for electrons, meaning C,N,S, and P want more electrons. This seems true, but then why does B usually only become BF3, meaning they do not want more electrons. B is true because it s.

Well first thing to remember is that C,N,S, and P.pdf

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They both have dipole-dipole interactions, intermolecular hydrogen bonding, and vander wals force. However, water has two lone pairs that can do hydrogen bonding whereas ammonia has only 1 lone pair. Solution They both have dipole-dipole interactions, intermolecular hydrogen bonding, and vander wals force. However, water has two lone pairs that can do hydrogen bonding whereas ammonia has only 1 lone pair..

They both have dipole-dipole interactions, interm.pdf

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The violin is a string instrument, usually with four strings tuned in perfect fifths. It is the smallest, highest-pitched member of the violin family of string instruments, which also includes the viola and cello. The violin is sometimes informally called a fiddle, regardless of the type of music played on it. The word violin comes from the Medieval Latin word vitula, meaning stringed instrument;this word is also believed to be the source of the Germanic \"fiddle\".The violin, while it has ancient origins, acquired most of its modern characteristics in 16th-century Italy, with some further modifications occurring in the 18th and 19th centuries. Violinists and collectors particularly prize the instruments made by the Gasparo da Sal Solution The violin is a string instrument, usually with four strings tuned in perfect fifths. It is the smallest, highest-pitched member of the violin family of string instruments, which also includes the viola and cello. The violin is sometimes informally called a fiddle, regardless of the type of music played on it. The word violin comes from the Medieval Latin word vitula, meaning stringed instrument;this word is also believed to be the source of the Germanic \"fiddle\".The violin, while it has ancient origins, acquired most of its modern characteristics in 16th-century Italy, with some further modifications occurring in the 18th and 19th centuries. Violinists and collectors particularly prize the instruments made by the Gasparo da Sal.

The violin is a string instrument, usually with f.pdf

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the element is phosphorus (P) Solution .pdf

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PV ^ n = constant using pv = N* R * T we get P ^ 1-n * T ^ n = contant T1= 150 T1= 293 P2= 600 T2 = 393 k P1/P2 = (T2/T1 ) ^ n/1-n 1/4 = ( 1.34)^ n/1-n taking log on both side log( 1/4) = n/1-n * ( log (1.34) n/1-n =-4.736 n= 1.267 Solution PV ^ n = constant using pv = N* R * T we get P ^ 1-n * T ^ n = contant T1= 150 T1= 293 P2= 600 T2 = 393 k P1/P2 = (T2/T1 ) ^ n/1-n 1/4 = ( 1.34)^ n/1-n taking log on both side log( 1/4) = n/1-n * ( log (1.34) n/1-n =-4.736 n= 1.267.

PV ^ n = constant using pv = N R T we get P ^ .pdf

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methyl-m-nitrobenzoate is more polar than methyl benzoate. There is a large separation of charge in the nitro group (between the nitrogen and oxygens). This leads to a higher level of polarity, and the compound containing the nitro is more polar. Hope this helps! Solution methyl-m-nitrobenzoate is more polar than methyl benzoate. There is a large separation of charge in the nitro group (between the nitrogen and oxygens). This leads to a higher level of polarity, and the compound containing the nitro is more polar. Hope this helps!.

methyl-m-nitrobenzoate is more polar than methyl .pdf

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L(f(t)) = 6s^4 - 2s^3 .pdf

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It was a 19th century geologist who first recognized periodicity in the physical properties of the elements. Alexandre Beguyer de Chancourtois (1820-1886), professor of geology at the School of Mines in Paris, published in 1862 a list of all the known elements. The list was constructed as a helical graph wrapped around a cylinder--elements with similar properties occupied positions on the same vertical line of cylinder (the list also included some ions and compounds). Using geological terms and published without the diagram, de Chancourtois ideas were completely ignored until the work of Mendeleev. it is used to distinguish elements by their properties Solution It was a 19th century geologist who first recognized periodicity in the physical properties of the elements. Alexandre Beguyer de Chancourtois (1820-1886), professor of geology at the School of Mines in Paris, published in 1862 a list of all the known elements. The list was constructed as a helical graph wrapped around a cylinder--elements with similar properties occupied positions on the same vertical line of cylinder (the list also included some ions and compounds). Using geological terms and published without the diagram, de Chancourtois ideas were completely ignored until the work of Mendeleev. it is used to distinguish elements by their properties.

It was a 19th century geologist who first recogni.pdf

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here the solution is 0.015 M HCl so we have HCl -.pdf

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H2SO4 + 2 NaOH = Na2SO4 + 2 H2O moles of NaOH = .pdf

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CCl4 4. molecular CaBr2 3. ionic RbF 3. ionic .pdf

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internet protocol stack contains 5 layers i)application layer ii)transport layer iii)network layer iv)link layer v)physical layer a) Route selection is done in network layer b)Provide user services such as e-mail and file transfer is done in application layer c) Mechanical and electrical interface is done in physical layer Solution internet protocol stack contains 5 layers i)application layer ii)transport layer iii)network layer iv)link layer v)physical layer a) Route selection is done in network layer b)Provide user services such as e-mail and file transfer is done in application layer c) Mechanical and electrical interface is done in physical layer.

internet protocol stack contains 5 layersi)application layerii)t.pdf

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in water, HC2H3O2 does not ionize since it is a weak acid CsOH, however, dissociates. Molecular: HC2H3O2(aq) + CsOH(aq) --> CsC2H3O2(aq) + H2O(l) Ionic: HC2H3O2(aq) + Cs+(aq) + OH-(aq) --> Cs+(aq) + C2H3O2-(aq) + H2O(l) Net Ionic: HC2H3O2(aq) + OH-(aq) --> C2H3O2-(aq) + H2O(l) Molecular fomula is where all compound are written as you would see them in reagent bottles. Ionic equation is where all compounds that dissociate in water are written as ions if in aqueous environment Net ionic equation is same as ionic equation, but species identical on both sides of equation (spectator ions) are not written. Hope it helps :D Solution in water, HC2H3O2 does not ionize since it is a weak acid CsOH, however, dissociates. Molecular: HC2H3O2(aq) + CsOH(aq) --> CsC2H3O2(aq) + H2O(l) Ionic: HC2H3O2(aq) + Cs+(aq) + OH-(aq) --> Cs+(aq) + C2H3O2-(aq) + H2O(l) Net Ionic: HC2H3O2(aq) + OH-(aq) --> C2H3O2-(aq) + H2O(l) Molecular fomula is where all compound are written as you would see them in reagent bottles. Ionic equation is where all compounds that dissociate in water are written as ions if in aqueous environment Net ionic equation is same as ionic equation, but species identical on both sides of equation (spectator ions) are not written. Hope it helps :D.

in water, HC2H3O2 does not ionize since it is a weak acid CsOH, ho.pdf

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In general, ligands are viewed as donating electrons andelectrostatic molecules to the central atom. Bonding is oftendescribed using the formalisms of molecular orbital theory. Ingeneral, electron pairs occupy the HOMO (Highest Occupied MolecularOrbital) of the ligands. Ligands and metal ions can be ordered in many ways; one rankingsystem focuses on ligand \'hardness\' (see also hard/soft acid/basetheory). Metal ions preferentially bind certain ligands. Ingeneral, \'hard\' metal ions prefer weak field ligands, whereas\'soft\' metal ions prefer strong field ligands. According to themolecular orbital theory, the HOMO of the ligand should have anenergy that overlaps with the LUMO (Lowest Unoccupied MolecularOrbital) of the metal preferential. Metal ions bound tostrong-field ligands follow the Aufbau principle, whereas complexesbound to weak-field ligands follow Hund\'s rule. Binding of the metal with the ligands results in a set ofmolecular orbitals, where the metal can be identified with a newHOMO and LUMO (the orbitals defining the properties and reactivityof the resulting complex) and a certain ordering of the 5d-orbitals (which may be filled, or partially filled withelectrons). In an octahedral environment, the 5 otherwisedegenerate d-orbitals split in sets of 2 and 3 orbitals (for a morein depth explanation, see crystal field theory). The energy difference between these 2 sets of d-orbitals iscalled the splitting parameter, o. The magnitudeof o is determined by the field-strength of theligand: strong field ligands, by definition, increaseo more than weak field ligands. Ligands can now besorted according to the magnitude of o (see thetable below). This ordering of ligands is almost invariable for allmetal ions and is called spectrochemical series. For complexes with a tetrahedral surrounding, the d-orbitalsagain split into two sets, but this time in reverse order: The energy difference between these 2 sets of d-orbitals is nowcalled t. The magnitude of t issmaller than for o, because in a tetrahedralcomplex only 4 ligands influence the d-orbitals, whereas in anoctahedral complex the d-orbitals are influenced by 6 ligands. Whenthe coordination number is neither octahedral nor tetrahedral, thesplitting becomes correspondingly more complex. For the purposes ofranking ligands, however, the properties of the octahedralcomplexes and the resulting o has been of primaryinterest. Solution In general, ligands are viewed as donating electrons andelectrostatic molecules to the central atom. Bonding is oftendescribed using the formalisms of molecular orbital theory. Ingeneral, electron pairs occupy the HOMO (Highest Occupied MolecularOrbital) of the ligands. Ligands and metal ions can be ordered in many ways; one rankingsystem focuses on ligand \'hardness\' (see also hard/soft acid/basetheory). Metal ions preferentially bind certain ligands. Ingeneral, \'hard\' metal ions prefer weak field ligands, whereas\'soft\' metal ions prefer strong field ligands. .

In general, ligands are viewed as donating electrons andelectrostati.pdf

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