1. True2.True3. False. TAQ polymerase is a type of polymerase wn.pdf

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A

1. True 2.True 3. False. TAQ polymerase is a type of polymerase wnich elongates DNA not ligase. 4.True 5.False \" ORI\" is the site of origin of replication where replication starts, 6.True 7.True 8.False. Reverse transcriptase is an enzyme that synthesizes DNA from RNA. 9.True 10. True 11.True Solution 1. True 2.True 3. False. TAQ polymerase is a type of polymerase wnich elongates DNA not ligase. 4.True 5.False \" ORI\" is the site of origin of replication where replication starts, 6.True 7.True 8.False. Reverse transcriptase is an enzyme that synthesizes DNA from RNA. 9.True 10. True 11.True.

1. True
2.True
3. False. TAQ polymerase is a type of polymerase wnich elongates DNA not ligase.
4.True
5.False " ORI" is the site of origin of replication where replication starts,
6.True
7.True
8.False. Reverse transcriptase is an enzyme that synthesizes DNA from RNA.
9.True
10. True
11.True
Solution
1. True
2.True
3. False. TAQ polymerase is a type of polymerase wnich elongates DNA not ligase.
4.True
5.False " ORI" is the site of origin of replication where replication starts,
6.True
7.True
8.False. Reverse transcriptase is an enzyme that synthesizes DNA from RNA.
9.True
10. True
11.True

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A. are aromatic because Benzene and Aromaticity Unusual stability of benzene, heat of hydrogenation versus trienes Pi molecular orbitals of benzene Huckel’s rules: aromatic anions and cations, aromaticity of heterocycles Cyclobutadiene, benzene, and Frost’s circle Electrophilic aromatic substitution, mechanism and energy diagrams Br2, Br2/FeBr3, nitration, sulfonation of benzene Friedel-Crafts alkylation and acylation, problems encountered Electrophilic aromatic substitution Directing groups in detail, resonance versus inductive effects, steric control Changing ortho / para directors to meta directors Addition and removal of directing/blocking groups and retrosynthetic analyses of highly substituted benzenes Electrophilic aromatic substitution of polycyclic aromatic compounds: napthlene and phenanthrene Heterocycles Aliphatic heterocycles & reactivities: aziridines versus epoxides and thioranes, synthesis and acidic activation of aziridines Aromatic heterocycles: acid-base properties of pyridine, pyrimidine, pyrrole, imidazole, etc. Electrophilic aromatic substitution reactivity and regioselectivity of pyrrole, furan, benzene, pyridine, etc. Synthesis of pyrroles, furan, and thiophene from ?-dicarbonyl compounds Furan and thiophene in Diels-Alder chemistry Fischer indole synthesis, regioselectivity of indoles in electrophilic aromatic substitution Pyridine as a base, a nucleophile, and an acyl transfer catalyst (DMAP) Pyridine in nucleophilic aromatic substitution: Chichibabin reaction and addition of PhLi Synthesis of pyridines: Hantzsch condensation Synthesis of quinolines and isoquinolines from anilines Solution A. are aromatic because Benzene and Aromaticity Unusual stability of benzene, heat of hydrogenation versus trienes Pi molecular orbitals of benzene Huckel’s rules: aromatic anions and cations, aromaticity of heterocycles Cyclobutadiene, benzene, and Frost’s circle Electrophilic aromatic substitution, mechanism and energy diagrams Br2, Br2/FeBr3, nitration, sulfonation of benzene Friedel-Crafts alkylation and acylation, problems encountered Electrophilic aromatic substitution Directing groups in detail, resonance versus inductive effects, steric control Changing ortho / para directors to meta directors Addition and removal of directing/blocking groups and retrosynthetic analyses of highly substituted benzenes Electrophilic aromatic substitution of polycyclic aromatic compounds: napthlene and phenanthrene Heterocycles Aliphatic heterocycles & reactivities: aziridines versus epoxides and thioranes, synthesis and acidic activation of aziridines Aromatic heterocycles: acid-base properties of pyridine, pyrimidine, pyrrole, imidazole, etc. Electrophilic aromatic substitution reactivity and regioselectivity of pyrrole, furan, benzene, pyridine, etc. Synthesis of pyrroles, furan, and thiophene from ?-dicarbonyl compounds Furan and thiophene in Diels-Alder chemistry Fischer indole synthesis, regioselectivity of indoles in electrophilic aroma.

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Answer 1 : Basic Earning per share Basic Earning per share = BE/BS = 25700/ 10600 = 2.42 Working Notes BE = Income available for common stock holders Net Income 50000 Less: Intt on Bonds (100000*6.5%) 6500 ------------- EBT 43500 Less Tax paid @ 30% 13050 ---------------- Income after tax 30450 Less Dividend paid to Prefered stock holder 4750 ------------------ Amount Available common 25700 Stock holder ----------- BS = Weighted avaerage no. of common stock = Share at begining 9600 May, 1 Share issued 1200 weight 1200 *8/12 800 SeP, 30 Share issued 800 Weight 800*3/12 200 ------------ Total no. of shares 10600 ----------------- Answer - 2 Dialute Earning Per share = Net Income/Avg shares+other convertible instuments = (50000-1950)/15100 = 48050/15100 = 3.18 Working notes Avg Share = 10600 Prefered stock (1000*2) = 2000 Bonds (100000/1000*25) = 2500 -------------------------- Total shares = 15100 --------------------------- Incremental EPS of Preferred Stock = 4750/2000 = 4750/2000 = 2.38 Incremental EPS of Bonds = interest/ incremental no. of shares due to conversion of bonds = 6500-1950/2500 = 4550/2500 = 1.82 Answer 3 Incremental Earning per share Bonds = $ 1.82 Preferred = $ 2.38 Solution Answer 1 : Basic Earning per share Basic Earning per share = BE/BS = 25700/ 10600 = 2.42 Working Notes BE = Income available for common stock holders Net Income 50000 Less: Intt on Bonds (100000*6.5%) 6500 ------------- EBT 43500 Less Tax paid @ 30% 13050 ---------------- Income after tax 30450 Less Dividend paid to Prefered stock holder 4750 ------------------ Amount Available common 25700 Stock holder ----------- BS = Weighted avaerage no. of common stock = Share at begining 9600 May, 1 Share issued 1200 weight 1200 *8/12 800 SeP, 30 Share issued 800 Weight 800*3/12 200 ------------ Total no. of shares 10600 ----------------- Answer - 2 Dialute Earning Per share = Net Income/Avg shares+other convertible instuments = (50000-1950)/15100 = 48050/15100 = 3.18 Working notes Avg Share = 10600 Prefered stock (1000*2) = 2000 Bonds (100000/1000*25) = 2500 -------------------------- Total shares = 15100 --------------------------- Incremental EPS of Preferred Stock = 4750/2000 = 4750/2000 = 2.38 Incremental EPS of Bonds = interest/ incremental no. of shares due to conversion of bonds = 6500-1950/2500 = 4550/2500 = 1.82 Answer 3 Incremental Earning per share Bonds = $ 1.82 Preferred = $ 2.38.

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