Homework Answers
Answer 25: We have filled the blanks with the names of reactant and products and enzymes in the glycolysis as follows:
Sl.No. Name of Reactant Name of Product Name of enzyme
(1) Glucose Glucose 6-phosphate Hexokinase
(2) Glucose 6-phosphate Fructose 6-phosphate Glucose 6-phosphate isomerase
(3) Fructose 6-phosphate Fructose 1,6-bisphosphate Phosphofructokinase-1
(4) Fructose 1,6-bisphosphate Dihydroxyacetone phosphate Fructose bisphosphate aldolase
+ Glyceraldehyde 3-phosphate
(5) Dihydroxyacetone phosphate Glyceraldehyde 3-phosphate Triosephosphate isomerase
(6) Glyceraldehyde 3-phosphate 1,3-bisphosphoglycerate Glyceraldehyde 3-phosphate dehydrogenase
(7) 1,3-bisphosphoglycerate 3-phosphoglycerate Phosphoglycerate kinase
(8) 3-phosphoglycerate 2-phosphoglycerate Phosphoglycerate mutase
(9) 2-phosphoglycerate Phosphoenolpyruvate Phosphopyruvate hydratase (Enolase)
(10) Phosphoenolpyruvate Pyruvate Pyruvate kinase
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25. Fill the blanks with the names of reactants/products and enzymes in the glycolysis (Please note...
rever; mbine - you 13.78 Identify the Fischer projection A to D that matches each of...
rever; mbine - you 13.78 Identify the Fischer projection A to D that matches each of the following: (13.1, 13.3) a. the L enantiomer of mannose b. a ketopentose c. an aldopentose d. a ketohexose о но СН,ОН НЕОН CHOH С=0 НЕОН H- С=0 НЕ ОН НО -н НО-н Но Hн НО -Н НЕОН НО - H н -ОН НОН CHOH СН,ОН СН,ОН CH,OH -ОН dic D
4.23,4.24 & 4.26 thank you 156 CHAPTER 4 Introduction to Organic Compounds Practice Problems 4.21 4.23...
4.23,4.24 & 4.26 thank you
156 CHAPTER 4 Introduction to Organic Compounds Practice Problems 4.21 4.23 Draw the condensed structural formula for each of the following alkyl groups: a. propyl b. methyl 4.24 Give the correct name for each of the following substituents: a. CH CH - b. CH3CH,CHCH- c. I- 4.25 Draw the skeletal structure for each of the following compounds: a. 2,3-dimethylpentane b. 2-ethyl-1,4-dimethylcyclohexane c. 1,2-dichlorohexane 4.26 Draw the skeletal structure for each of the following compounds: a....
1A) What type of reaction occurs at 2? phosphorylation Isomerization hydrolysis oxidation-reduction dephosphorylatioN 1B) What type...
1A) What type of reaction occurs at 2?
phosphorylation
Isomerization
hydrolysis
oxidation-reduction
dephosphorylatioN
1B) What type of reaction occurs at 7?
phosphorylation
Isomerization
hydrolysis
oxidation-reduction
dephosphorylation
A B CHO он с CH, OH D Нc-o-Po, сно -он н го о H HO -н 2 но- -H 3 н- -он H но -H н -он н -он нс-о-ро, он он но H H -он н он нс-о-ро, н -он н CH,OH нс-о-ро, H G ОРО, 7 6 F E CHO нс-о-РО,...
Biochemistry. Please answer all completely. 13. Identify the electrophilic center and nucleophile in the below image...
Biochemistry. Please answer all completely.
13. Identify the electrophilic center and nucleophile in the below image : R 14. Give an example of amino acids with R group shown below which can function as nucleophile during enzyme catalysis. Nucleophiles Negatively charged oxygen (as in an unprotonated hydroxyl group or an ionized carboxylic acid) Negatively charged sulfhydryl Uncharged amine group HN Imidazole 15. Identify the amino acids with the following side chains and also define if they will work as acid...
Classify the following compounds as reducing sugars, non-reducing sugars, or neither: CH2OH CH2OH HONO CH2OH НО...
Classify the following compounds as reducing sugars, non-reducing sugars, or neither: CH2OH CH2OH HONO CH2OH НО НО CH2OH CH2OH НО- ONOH но но- HONO CH2OH но. HONO но от OCH3 OH но- ОН OH HO A с но но сHOH но снон CH OH CH2OH HONO ноу. НОА но -о но I H NH₂ HO но ОН N o="cs но і HO Но, IZ но го Е сн,он 1. non-reducing sugar - АА. C- B 2. reducing sugar - с...
Can someone please help fill in the blanks in these metabolism reactions? 1. Oxidation-reduction: Aoxidized +...
Can someone please help fill in the blanks
in these metabolism reactions?
1. Oxidation-reduction: Aoxidized + Breduced - A reduced + Boxidized Example: HC=0 H-C-OH H-C-OH + reduction H-C-OH H-C-OH 2. Group transfer: A-X + B-H — A-H+ B-X Example: H₂C-OH H-C-OH H-C-OH + NH2 H-C-OH H-C-OH I-O- group transfer 0 0 NN -o-R-o-P-oyo 0-0-00 0=4-00 to-o-P-oyo ОН ОН 3. Hydrolytic cleavage: A-B + H20 — A-OH+ B-H Example: HO OH нон HO OH нон Ho Ано 1-0 hydrolysis HO...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23,...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23, 4.24, 4.26 pg 170 - 4.29, 4.31, pg 171-4.36 pg 175 - 4.59 pg 176- 4.74, 4.75, 4.80 pg 177-4.81, 4.82 pg 188- 5.1, 5.4, 5.5, 5.6, 5.11 - Using Table 5.1 pg 198-5.22, 5.25 pg 203 - 5.29 pg 206 - 5.37 pg 209 - 5.39 pg 2.14 5.61 pg 235-6.11, 6.14, 6.16 156 CHAPTER 4 Introduction to Organic Compounds...
Name the following aldoses. (Include in the names the stereochemical designation D or L and, where...
Name the following aldoses. (Include in the names the stereochemical designation D or L and, where appropriate, the configuration of the anomeric carbon, alpha or beta. This question is case-sensitive, so capitalize only the D or L.) ball & stick + labels b all & stick + labels The following model is that of an aldopentose: ball & stick - + labels Draw the alpha anomer of the sugar in its furanose form. Classify each of the following sugars. (For...
Calculate the standard change in Gibbs free energy for the reaction at 25 °C. Standard Gibbs...
Calculate the standard change in Gibbs free energy for the reaction at 25 °C. Standard Gibbs free energy of formation values can be found in this table. 6 Cl(g)+2 Fe,O,(s)4 FeCl, (s)+30,(g) kJ/mol AGn= Thermodynamic Properties at 298 K Organic Compounds AG kJ/mol /(mol-K) дне kJ/mol Substance Name Formula дне kJ/mol Ag(s) Ag (aq) Ag20(s) Ag2S(s) AgBr(s) AgC(s) Agl(s) AgNO3(s) Al(s) Al2O3(s) AICI3(s) 0 42.6 105.8 77.107 73.4 Methane CH4(9) СHа(о) -74.6) -84.0 -103.8 -11.2 -31.1 121.3 Ethane -32.6 -40.7...
rever; mbine - you 13.78 Identify the Fischer projection A to D that matches each of the following: (13.1, 13.3) a. the L enantiomer of mannose b. a ketopentose c. an aldopentose d. a ketohexose о но СН,ОН НЕОН CHOH С=0 НЕОН H- С=0 НЕ ОН НО -н НО-н Но Hн НО -Н НЕОН НО - H н -ОН НОН CHOH СН,ОН СН,ОН CH,OH -ОН dic D
4.23,4.24 & 4.26 thank you
156 CHAPTER 4 Introduction to Organic Compounds Practice Problems 4.21 4.23 Draw the condensed structural formula for each of the following alkyl groups: a. propyl b. methyl 4.24 Give the correct name for each of the following substituents: a. CH CH - b. CH3CH,CHCH- c. I- 4.25 Draw the skeletal structure for each of the following compounds: a. 2,3-dimethylpentane b. 2-ethyl-1,4-dimethylcyclohexane c. 1,2-dichlorohexane 4.26 Draw the skeletal structure for each of the following compounds: a....
1A) What type of reaction occurs at 2?
phosphorylation
Isomerization
hydrolysis
oxidation-reduction
dephosphorylatioN
1B) What type of reaction occurs at 7?
phosphorylation
Isomerization
hydrolysis
oxidation-reduction
dephosphorylation
A B CHO он с CH, OH D Нc-o-Po, сно -он н го о H HO -н 2 но- -H 3 н- -он H но -H н -он н -он нс-о-ро, он он но H H -он н он нс-о-ро, н -он н CH,OH нс-о-ро, H G ОРО, 7 6 F E CHO нс-о-РО,...
Biochemistry. Please answer all completely.
13. Identify the electrophilic center and nucleophile in the below image : R 14. Give an example of amino acids with R group shown below which can function as nucleophile during enzyme catalysis. Nucleophiles Negatively charged oxygen (as in an unprotonated hydroxyl group or an ionized carboxylic acid) Negatively charged sulfhydryl Uncharged amine group HN Imidazole 15. Identify the amino acids with the following side chains and also define if they will work as acid...
Classify the following compounds as reducing sugars, non-reducing sugars, or neither: CH2OH CH2OH HONO CH2OH НО НО CH2OH CH2OH НО- ONOH но но- HONO CH2OH но. HONO но от OCH3 OH но- ОН OH HO A с но но сHOH но снон CH OH CH2OH HONO ноу. НОА но -о но I H NH₂ HO но ОН N o="cs но і HO Но, IZ но го Е сн,он 1. non-reducing sugar - АА. C- B 2. reducing sugar - с...
Can someone please help fill in the blanks
in these metabolism reactions?
1. Oxidation-reduction: Aoxidized + Breduced - A reduced + Boxidized Example: HC=0 H-C-OH H-C-OH + reduction H-C-OH H-C-OH 2. Group transfer: A-X + B-H — A-H+ B-X Example: H₂C-OH H-C-OH H-C-OH + NH2 H-C-OH H-C-OH I-O- group transfer 0 0 NN -o-R-o-P-oyo 0-0-00 0=4-00 to-o-P-oyo ОН ОН 3. Hydrolytic cleavage: A-B + H20 — A-OH+ B-H Example: HO OH нон HO OH нон Ho Ано 1-0 hydrolysis HO...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23, 4.24, 4.26 pg 170 - 4.29, 4.31, pg 171-4.36 pg 175 - 4.59 pg 176- 4.74, 4.75, 4.80 pg 177-4.81, 4.82 pg 188- 5.1, 5.4, 5.5, 5.6, 5.11 - Using Table 5.1 pg 198-5.22, 5.25 pg 203 - 5.29 pg 206 - 5.37 pg 209 - 5.39 pg 2.14 5.61 pg 235-6.11, 6.14, 6.16 156 CHAPTER 4 Introduction to Organic Compounds...
Name the following aldoses. (Include in the names the stereochemical designation D or L and, where appropriate, the configuration of the anomeric carbon, alpha or beta. This question is case-sensitive, so capitalize only the D or L.) ball & stick + labels b all & stick + labels The following model is that of an aldopentose: ball & stick - + labels Draw the alpha anomer of the sugar in its furanose form. Classify each of the following sugars. (For...
Calculate the standard change in Gibbs free energy for the reaction at 25 °C. Standard Gibbs free energy of formation values can be found in this table. 6 Cl(g)+2 Fe,O,(s)4 FeCl, (s)+30,(g) kJ/mol AGn= Thermodynamic Properties at 298 K Organic Compounds AG kJ/mol /(mol-K) дне kJ/mol Substance Name Formula дне kJ/mol Ag(s) Ag (aq) Ag20(s) Ag2S(s) AgBr(s) AgC(s) Agl(s) AgNO3(s) Al(s) Al2O3(s) AICI3(s) 0 42.6 105.8 77.107 73.4 Methane CH4(9) СHа(о) -74.6) -84.0 -103.8 -11.2 -31.1 121.3 Ethane -32.6 -40.7...
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