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The substance which gains electron are reduced itself while which lose electron oxidize itself.
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5.59 Provide the products and balance the following reac tion for the complete combustion of pentane,...
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....
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...
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
Carbohydrates 1. Label each of the monosaccharides shown below as a triose, tetrose, pentoso, or hexose....
Carbohydrates 1. Label each of the monosaccharides shown below as a triose, tetrose, pentoso, or hexose. но CH OH HT -он - он Н - ОН но -н но -Н но -н нон сньон он но -н НОН CH OH нон нон нон снон CH OH сон сон H- OH H- -он OH cң, он н-с-он Сн,он снон 2. Label each of the monosaccharides shown above as a ketose or aldose. 3. Identify all of the chiral carbons in the...
4. For each sugar below, characterize the anomer if a monosaccharide or the glycosidic bond(s) if...
4. For each sugar below, characterize the anomer if a monosaccharide or the glycosidic bond(s) if a di- or polysaccharide (e.g., B,B-2,3; if there is more than one glycosidic bond, draw an arrow from each label to its corresponding bond). CH,OH CH2OH CH OН но н H Н H Он Н OH н OH Он Н ОН O H Но он b. a. OH H OH CH-OH O H Но ОН Н CH2OH CH2 CH2OH он OCH CH3 Но н...
1. For each of the following sugars: state the classification (by number of carbons and carbonyl type, like aldotetr...
1. For each of the following sugars: state the classification (by number of carbons and carbonyl type, like aldotetrose), whether the sugar is D- or L-form, and draw the enantiomer. но СН,ОН н-с- OH но-с-н н-с- он нс- он CH OH с=0 но -н нон но -н СН,ОН CH2OH 1 С=0 но но НО -н -н -н CHOH н-с- он CH OH
Q1: CH, OH CHOH HO X OH OH OH a. Give common name of the given...
Q1: CH, OH CHOH HO X OH OH OH a. Give common name of the given sugars. b. Name the glycoside linkage c. Identify them and reducing or non-reducing sugars d. Write the product for hydrolysis of these disaccharides Q 2: (a) Identify the type of isomers: СНО СНО но НО —н -н нон н — — ОН СН,ОН СН,ОН
Question 2 Identify all D-monosaccharides below: CHO НЕОН НОН Н -ОН НОНЕН CHO НО. -Н НОН...
Question 2 Identify all D-monosaccharides below: CHO НЕОН НОН Н -ОН НОНЕН CHO НО. -Н НОН НО-НН НО. -Н НО -Н CH2OH ІІ H Н ОН 0= НО-Н НЕОН Н ОН CH2OH CHO Н- -ОН НОН НЕОН НО-Н НЕОН CH OH IV — о Н- НОНЕН Н- ОН НО-Н Н ОН НО НО- CH2OH Ео Н ОН -Н -Н Н. -ОН Н VI CH2OH H ОН 0 Н- НО. -Н НО -Н Н VII Н Нон 0= НЕОН НО-НН НО....
30. Which of the choices below is the enantiomer of D-glucose? сно сно нон HO-EH сно...
30. Which of the choices below is the enantiomer of D-glucose? сно сно нон HO-EH сно на-он D-glucose Іно-Ен н -он но-Ен EH,OH сно но н-он но -н нон Сн,он но-Ен на-он но -н но-Ен н -он нон CHO но -н н-он но-Ен нон снен CHOH Сн,он 3. Which of the following structures is an a-anomer? Сн,он —о, он o ноноон нонс осн он — о оно сн, он он онон он он он он тон КСн,он y CH, OH...
Culhydrates 1. Complete th Complete the table by classifying each sugar sugar (A, B, C, D)...
Culhydrates 1. Complete th Complete the table by classifying each sugar sugar (A, B, C, D) below based on carbonyl group and number of carbons (c.8. aldohexose, ketotriose, etc.). Classify them as an antiomer. Indicate the number of chiral carbons for each sugar. Sugar Classification based on carbonyl group and number of carbons Lor D enantiomer Number of chiral carbons н-с-он HO-6-H. н-с-он ін,он CH,OH C=0 HO-C-H н-с-он HO-C-H. ён,он снон c=0 | HO-C-H ін,он H-C-OH CH, OH CD 2....
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....
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...
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
Carbohydrates 1. Label each of the monosaccharides shown below as a triose, tetrose, pentoso, or hexose. но CH OH HT -он - он Н - ОН но -н но -Н но -н нон сньон он но -н НОН CH OH нон нон нон снон CH OH сон сон H- OH H- -он OH cң, он н-с-он Сн,он снон 2. Label each of the monosaccharides shown above as a ketose or aldose. 3. Identify all of the chiral carbons in the...
4. For each sugar below, characterize the anomer if a monosaccharide or the glycosidic bond(s) if a di- or polysaccharide (e.g., B,B-2,3; if there is more than one glycosidic bond, draw an arrow from each label to its corresponding bond). CH,OH CH2OH CH OН но н H Н H Он Н OH н OH Он Н ОН O H Но он b. a. OH H OH CH-OH O H Но ОН Н CH2OH CH2 CH2OH он OCH CH3 Но н...
1. For each of the following sugars: state the classification (by number of carbons and carbonyl type, like aldotetrose), whether the sugar is D- or L-form, and draw the enantiomer. но СН,ОН н-с- OH но-с-н н-с- он нс- он CH OH с=0 но -н нон но -н СН,ОН CH2OH 1 С=0 но но НО -н -н -н CHOH н-с- он CH OH
Q1: CH, OH CHOH HO X OH OH OH a. Give common name of the given sugars. b. Name the glycoside linkage c. Identify them and reducing or non-reducing sugars d. Write the product for hydrolysis of these disaccharides Q 2: (a) Identify the type of isomers: СНО СНО но НО —н -н нон н — — ОН СН,ОН СН,ОН
Question 2 Identify all D-monosaccharides below: CHO НЕОН НОН Н -ОН НОНЕН CHO НО. -Н НОН НО-НН НО. -Н НО -Н CH2OH ІІ H Н ОН 0= НО-Н НЕОН Н ОН CH2OH CHO Н- -ОН НОН НЕОН НО-Н НЕОН CH OH IV — о Н- НОНЕН Н- ОН НО-Н Н ОН НО НО- CH2OH Ео Н ОН -Н -Н Н. -ОН Н VI CH2OH H ОН 0 Н- НО. -Н НО -Н Н VII Н Нон 0= НЕОН НО-НН НО....
30. Which of the choices below is the enantiomer of D-glucose? сно сно нон HO-EH сно на-он D-glucose Іно-Ен н -он но-Ен EH,OH сно но н-он но -н нон Сн,он но-Ен на-он но -н но-Ен н -он нон CHO но -н н-он но-Ен нон снен CHOH Сн,он 3. Which of the following structures is an a-anomer? Сн,он —о, он o ноноон нонс осн он — о оно сн, он он онон он он он он тон КСн,он y CH, OH...
Culhydrates 1. Complete th Complete the table by classifying each sugar sugar (A, B, C, D) below based on carbonyl group and number of carbons (c.8. aldohexose, ketotriose, etc.). Classify them as an antiomer. Indicate the number of chiral carbons for each sugar. Sugar Classification based on carbonyl group and number of carbons Lor D enantiomer Number of chiral carbons н-с-он HO-6-H. н-с-он ін,он CH,OH C=0 HO-C-H н-с-он HO-C-H. ён,он снон c=0 | HO-C-H ін,он H-C-OH CH, OH CD 2....
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