Nun im Themenbereich OC_en
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- Drawing Various functional Groups (oc-01)Drawing to the each exercise in each case three various molecules, which It 's just … from a Hydrogen-carbon rigs (Alkaline scaffolds, So what do you mean? Inland waterways) and the following: functional Group of which::
- I 'm not . Branched Alkanes
- Branched Alkanes
- Cyclic Alkanes
- Alkenes
- Alkyne
- Alcohol
- aldehyde
- ketone
- Amina
- carboxylic acid
- amino acid
- ester
- amide
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- Drawing Various functional Groups, 2 (oc-02)Drawing to each exercise The Structural formula. In addition The Functional Group may No Other Functional Groups drawn will be, permitted are It 's just … Not yet Coal-hydrogen linkages
- One of them Linear, not of branches Alcohol with Exactly . 3 Carbon atoms
- One of them of branches Alcohol with Exactly . 5 Carbon atoms
- All of them Alcohol (Branched, not Branched) with Exactly . 4 Carbon atoms
- Three of them various ether with in each case In total 4 Carbon atoms
- This the smallest possible (This is it. a few C How feasible) ketone
- This the smallest possible (This is it. a few C How feasible) aldehyde
- This the smallest possible (This is it. a few C How feasible) Amina
- The the smallest possible (This is it. a few C How feasible) ester
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- Drawing Various functional Groups, 3 (oc-03)Drawing in each case a of any kind molecule, which At the same time All of them Functional Groups Includes, The Basic structure It should be Always a Fresh or chilled be
- alkene, Alcohol and carboxylic acid
- alkene, aldehyde, ketone and amide
- carboxylic acid, Alcohol and ketone
- Amina, amide, carboxylic acid and Aldeyhd
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- Drawing Different Alcohol (oc-04)Drawing in each case three various Alcohol:
- Primary Alcohol
- secondary Alcohol
- Tertiary Alcohol
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- Drawing Different Alcohol, 2 (oc-05)All of them to Drawing molecule must four Carbon atoms have. Drawing with This Specifications The Commission One
…. Primary Alcohol, secondary Alcohol and Tertiary Alcohol. - 1
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- nomenclature, molecules drawing, 1 (oc-10)Given are the following: 6 molecules. One of them of which: is distinct The Commission Unambiguous of All of them Other. What ? and Why ??{a) } \<|>/<`|>\/\/\{b) } /<`|>\<|>/\/\|{c) } \/\/\<|<`/>\>/{d) } /<`|>\<|>/\/\/{e) } \/\|`/<`\>|<`/>\{f) } \|`/|<`/>\/<`|>\
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- nomenclature, molecules drawing, 2 (oc-11)Given are the following: Names various molecules. Drawing This of which: molecule (Skeletal spelling).
- Hexan
- 2-Methyl octane
- 3,4-The Commission-Ethyl-2,2,5-Tri-methyl decane
- Ethanol (also Ethan-1-Ol)
- Propan-1,2,3-Tri-ol
- Butan-1-Other
- Butan-2-on
- Cyclohexanol
- 4-Methyl-Pentan-1-Ol
- 2-Methyl-Pentan-2-Ol
- 3-Amino-Heptan-1-Ol
- 3-Hydroxy butaneal
- 2,3-Dimethyl-Butan-2,3-diol
- 2,3-Dimethyl pentane
- 1-Ethyl-1-Methyl cyclobutan
- 3-Ethyl-2,2,4-Tri-methyl hexane
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- nomenclature, Molecular names to determine (oc-12)Given are the following: Structures various molecules. Turn around . The Rules of nomenclature as far as possible Exactly . to and Give The systematically Names.{a) } -_(P3)_(P3)<`/>`\{b) } /<`|><_(A75)>\/{c) } \/<`|>\/\<_p3><\>/{d) } @:n(n,a,L:.4)<_(A&a,L&L,N0)$itemColor1(white)\"&n\">@; @n(9,90)/@n(8,90)\@n(7,90)/@n(6,90)\@n(5,-90)|@n(4,90)<`/|>\@n(3,-90)<|>/@n(2,90)<\>`|@n(1,-90){e) } @:n(n,a,L:.4)<_(A&a,L&L,N0)$itemColor1(white)\"&n\">@; @n(5,90)/@n(4,90)<`|O|>\@n(3,90)/@n(2,90)\@n(1,-90)|O`|{f) } \/<`|>\<|<`/>\NH2>/OH{g) } /\/<`|>\\/>|<`/>\<|OH>/\<|>/NH2{h) } HO/<`|O|>\/<`|>\<|`/<`\H2N>|<`/>\>/\{i) } /<`|>\/\/{j) } /<`|>\<|>/<`|>\{k) } /\<|>/\/\{l) } /\<_(A150)><|OH>/\{m) } Br\<|>/\/
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- nomenclature, chirality (oc-20)Given are the following: molecules. Should This molecule a or several Chirality centres contained, This is it. mark These with a The stars. Should No Chirality centres to to find be, This is it. It should be The Indication kC (No Chirality centres) made will be.{a: } /<`|>\/\/{b: } /<`|>\<|>/<`|>\{c: } /\<|>/\/\{d: } /\<_(A150)><|OH>/\{e: } Br\<|>/\/{f: } OH`\`|O|`/|`/`\`|//\|\O|`/O/\{g: } –<_(a30,N2)O>_q3O_q3<>_(a30){h: } OH|`/|<\OH>`/<|OH>`\<`/HO>`|`\O\/O\{i: } `/O`\`/O/`|//\|\/`||`\`//{j: } ||`/`\<`/HO>`|<`\HO>//\/<_(A-90)OH>\/N<_(y-.5)H>\CH3{j: } \|`//<|>`\`/O/`|/`|`\c\/{j: } `|/:a\|_#1`/`\`/<`|>|`/`\<`/HO>`|/\|0\/`|`\0`|/\`|; #a`|<`\>/\/\<|>/
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- nomenclature, chirality, 2 (oc-21)Drawing three molecules, which in each case at least: a Chirality centre have. The drawn molecules must be Neutral be. Indicators The Chirality centres in each case with a The stars.
Partial task a) All of them Elements are permitted
Partial task b) in to each molecule must be The Elements C, H and Br at least: One time occurring, Other Elements are not permitted. - 1
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- Oxidation road 1 (oc-30)Oxidants the following: Substances in each case One time. Give it away In the case of each Oxidation This It ‘s just … short-term The following is an extract: Intermediate product to. Example:
{a) } /\OH->[/<`|OH>\OH]->/\O`\ + H2O{b) } \<|>/\OH{c) } /\<|HO>/{d) } /<`|>\/<`|OH>\/{e) } OH|_(A75);/#2\ - 1
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- Oxidation road 2 (oc-31)Oxidants the following: Alcohol in so far as How possible.{a) } /\OH{b) } \<|>/\OH{c) } \/<`|>\/OH{d) } /\<|HO>/{e) } \/<`|OH>\|{f) } /<`|>\/<`|OH>\/{g) } OH|_(A75);/#2\{h) } OH|_(A75);/#2\/`|{i) } OH|_(A75);/#2\/\|
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- Oxidation road 3 (oc-32)Given are the following: Alcohol. Oxidants – where applicable possible – All of them Alcohol One time.{a) } /\OH{b) } \<|>/\OH{c) } \/<`|>\/OH{d) } HO\/<`|OH>\/OH{e) } `|/:a\|_#1`/`\`/<`|>|`/`\<`/HO>`|/\|0\\/`|`\0`|/\`|; #a`|<`\>/\/\<|>/{f) } `/`-`\/-<\>\-OH{g) } `/`-`\/-\-OH{h) } HO\<|>/<`|NH2>\<|OH>/<`|OH>\<_(A45)><_(A-220)>/OH{i) } HO|`/|`/`\\`|<`\<_q><_(A-70)OH>`\>//\|\O/\\/<\O/\OH>`||`\`//|{j) } OH`\`|O|`/|`/`\\`|<`\`/HO>//\|\O|`/O/\
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- retrosynthesis, Reduction (oc-35)Given are the following: Structures. How can The Substances from The This is the case for Hydrogenated hydrocarbons Manufacture will be? Write The This is the case for (Stable) Intermediate steps I ‘m going .. To the Part of must to The the right Place Reduced (Responsibility. Oxidated) will be, These Technical Difficulties Applicable It ‘s But to This Place not to take into account.
Sample solution given In the case of Example a). Please note: also, that The Notation with a Retrosynthesis arrow made has been. Go on . by analogy before.{a) } /\/`|O|\OH⇒ /\/`|O|\H⇒ /\/`|OH⇒ /\/{b) } \<|>/`|O|\H{c) } \/<`|>\|O`|/OH{d) } /<`|>\/<`|O|>\/{e) } OH|_(A75);/#2\ - 1
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- Functional Groups with each other reacting to leave, Condensation reactions 1 (oc-40)Given are the following: molecules. Let it go. These in One of them condensation reaction with each other reacting.{a) Two equal to Alcohol }{a1) } /\/OH + /\/OH{a2) } \<|>/\OH + \<|>/\OH{a3) } \/<`|>\/OH + HO\/<`|>\/{a4) } /<`|>\/<`|OH>\/ + /<`|>\/<`|OH>\/{a5) } OH|_(A75);/#2\ + |_(A75);HO/#2\{a6) } 2* \<|>/<`|OH>\{b) Two various Alcohol }{b1) } /\OH + HO/{b2) } /<`|OH>\ + /\OH{b3) } \<|>/<`|OH>\ + /\OH{c) Alcohol and One carboxylic acid }{c1) } \/\OH + HO/<`|O|>\{c2) } \<|>/<`|OH>\ + HO/<`|O|>\<|>/{c3) } /\<|O`|>/OH + \<|>/<`|OH>{d) Two equal to carboxylic acid }{d1) } /<`|O|>\OH + HO/<`|O|>\{d2) } 2* $C()|O`|/OH{d3) } 2* `/`\`|/\|\/`|O|\OH{e) Two various carboxylic acid }{e1) } /\<|O`|>/OH + HO/`|O|{e2) } HO\|O`|/<`|>\/ + \/`|O|\OH{e3) } HO\|O`|/<`|>\ + /`|O|\OH{f) Amina and One carboxylic acid }{f1) } /NH2 + HO/`|O|\{f2) } \<|>/NH2 + /\|O`|/OH{f3) } \<|>/N<_(y-.5)H>\ + /\|O`|/OH
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- Functional Groups with each other reacting to leave, Condensation reactions 2 (oc-41)Go on . In the case of each exercise The following masses before:
– Drawing The requested(n) molecules with The Functional Groups
– Let it go. The Both drawn molecules with each other reacting
– In addition to the Product Water is generated One new functional Group. What ??
– Each of them Partial task It should be at least: three times solved will be
Notes: The molecules to be Neutral be- Two identical Alcohol reacting with each other
- Two Different Alcohol reacting with each other
- One of them Alcohol reacts with One of them carboxylic acid
- Two identical Carbonic acids reacting with each other
- Two Different Carbonic acids reacting with each other
- One of them Amina reacting with One of them carboxylic acid
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- Functional Groups with each other reacting to leave, Condensation reactions 3 (oc-42)Es are the following: Products of condensation reaction given. Drawing The Scalpeline formulas The This is the case for Educated by analogy to the the first Example. Please note:, that The Notation with a Retrosynthesis arrow made has been. Go on . by analogy before.{a1) } /\/O\/\
+ H2O⇒ /\/OH + HO\/\{a2) } \<|>/\O/\<|>/+ H2O{a3) } \/<`|>\/O\/<`|>\/+ H2O{a4) } /<`|>\/<`|O/<`|/<`|>\>\/>\/+ H2O{a5) } $C()/<_(A225)><_(A-45)>\O/<_(A225)><_(A-45)>\+ H2O{a6) } \<|>/<`|>\O/<`|>\<|>/+ H2O{b1) } /\O/+ H2O{b2) } /<`|>\O/\+ H2O{b3) } \<|>/<`|>\O/\+ H2O{c1) } \/\O/<`|O|>\+ H2O{c2) } \<|>/<`|>\O/<`|O|>\<|>/+ H2O{c3) } /\<|O`|>/O\/<`|>\+ H2O{c4) } -_qO_q<`|O|>_q_q+ H2O{d1) } /<`|O|>\O/<`|O|>\+ H2O{d2) } `|O|\O/`|O|+ H2O{d3) } `/`\`|/\|\/`|O|\O/`|O|\/`|/\|`/`\+ H2O{e1) } \/`|O|\O/`|O|+ H2O{e2) } \/`|O|\O/`|O|\<|>/\+ H2O{e3) } /`|O|\O/`|O|\<|>/+ H2O{f1) } /N<_(y-.5)H>\|O`|/+ H2O{f2) } \<|>/N<_(y-.5)H>\|O`|/\+ H2O{f3) } \<|>/N<`|>\|O`|/\+ H2O{f4) } -_qNH_q<`|O|>_q_q+ H2O - 1
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- Structure Predictions, exercise 1 (oc-50)Given are the following: Results One of them elemental analysis: C 12.79%. H 2.15%, The Remains be Bromine
- How is The molecular formula
- Drawing This molecule by: The molecular formula. What ? falling on?
- How See ? This to Expected NMR The (Both!) Structures from?
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