(a)
Interpretation:
Fischer projection for given compounds should be drawn.
Concept introduction:
The Fischer projection: Fischer projection is a two-dimensional representation of a three-dimensional organic molecule by projection. It is mainly proposed for the representation of carbohydrate chemistry.
The orientation of the carbon atoms in a molecule is arranged vertically from top to bottom.
The C1 carbon is at the top of the orientation, the hydrogen and hydroxyl groups are placed in right and left side of the orientation. D and L form are depends on the arrangement of the hydroxyl group. If the hydroxyl group is in the right side of the molecule in the penultimate (next-to-last) carbon is called as D sugar, if the If the hydroxyl group is in the left side of the molecule in the penultimate (next-to-last) carbon is called as L sugar.
The molecular formula for the sugar unit is C6H12O6.
To find: Fischer projection for given molecule
(b)
Interpretation:
Fischer projection for given compounds should be drawn.
Concept introduction:
The Fischer projection: Fischer projection is a two-dimensional representation of a three-dimensional organic molecule by projection. It is mainly proposed for the representation of carbohydrate chemistry.
The orientation of the carbon atoms in a molecule is arranged vertically from top to bottom.
The C1 carbon is at the top of the orientation, the hydrogen and hydroxyl groups are placed in right and left side of the orientation. D and L form are depends on the arrangement of the hydroxyl group. If the hydroxyl group is in the right side of the molecule in the penultimate (next-to-last) carbon is called as D sugar, if the If the hydroxyl group is in the left side of the molecule in the penultimate (next-to-last) carbon is called as L sugar.
The molecular formula for the sugar unit is C6H12O6.
To find: Fischer projection for given molecule
(c)
Interpretation:
Fischer projection for given compounds should be drawn.
Concept introduction:
The Fischer projection: Fischer projection is a two-dimensional representation of a three-dimensional organic molecule by projection. It is mainly proposed for the representation of carbohydrate chemistry.
The orientation of the carbon atoms in a molecule is arranged vertically from top to bottom.
The C1 carbon is at the top of the orientation, the hydrogen and hydroxyl groups are placed in right and left side of the orientation. D and L form are depends on the arrangement of the hydroxyl group. If the hydroxyl group is in the right side of the molecule in the penultimate (next-to-last) carbon is called as D sugar, if the If the hydroxyl group is in the left side of the molecule in the penultimate (next-to-last) carbon is called as L sugar.
The molecular formula for the sugar unit is C6H12O6.
To find: Fischer projection for given molecule
(d)
Interpretation:
Fischer projection for given compounds should be drawn.
Concept introduction:
The Fischer projection: Fischer projection is a two-dimensional representation of a three-dimensional organic molecule by projection. It is mainly proposed for the representation of carbohydrate chemistry.
The orientation of the carbon atoms in a molecule is arranged vertically from top to bottom.
The C1 carbon is at the top of the orientation, the hydrogen and hydroxyl groups are placed in right and left side of the orientation. D and L form are depends on the arrangement of the hydroxyl group. If the hydroxyl group is in the right side of the molecule in the penultimate (next-to-last) carbon is called as D sugar, if the If the hydroxyl group is in the left side of the molecule in the penultimate (next-to-last) carbon is called as L sugar.
The molecular formula for the sugar unit is C6H12O6.
To find: Fischer projection for given molecule
Want to see the full answer?
Check out a sample textbook solution
Chapter 24 Solutions
ORGANIC CHEMISTRY 2-SEMESTER-ACCESS
- 1. Show the steps necessary to make 2-methyl-4-nonene using a Wittig reaction. Start with triphenylphosphine and an alkyl halide. After that you may use any other organic or inorganic reagents. 2. Write in the product of this reaction: CH3 CH₂ (C6H5)₂CuLi H₂O+arrow_forward3. Name this compound properly, including stereochemistry. H₂C H3C CH3 OH 4. Show the step(s) necessary to transform the compound on the left into the acid on the right. Bri CH2 5. Write in the product of this LiAlH4 Br H₂C OHarrow_forwardWhat are the major products of the following reaction? Please provide a detailed explanation and a drawing to show how the reaction proceeds.arrow_forward
- What are the major products of the following enolate alkylation reaction? Please include a detailed explanation as well as a drawing as to how the reaction proceeds.arrow_forwardA block of zinc has an initial temperature of 94.2 degrees celcius and is immererd in 105 g of water at 21.90 degrees celcius. At thermal equilibrium, the final temperature is 25.20 degrees celcius. What is the mass of the zinc block? Cs(Zn) = 0.390 J/gxdegrees celcius Cs(H2O) = 4.18 J/gx degrees celcusarrow_forwardPotential Energy (kJ) 1. Consider these three reactions as the elementary steps in the mechanism for a chemical reaction. AH = -950 kJ AH = 575 kJ (i) Cl₂ (g) + Pt (s) 2C1 (g) + Pt (s) Ea = 1550 kJ (ii) Cl (g)+ CO (g) + Pt (s) → CICO (g) + Pt (s) (iii) Cl (g) + CICO (g) → Cl₂CO (g) Ea = 2240 kJ Ea = 2350 kJ AH = -825 kJ 2600 2400 2200 2000 1800 1600 1400 1200 1000 a. Draw the potential energy diagram for the reaction. Label the data points for clarity. The potential energy of the reactants is 600 kJ 800 600 400 200 0 -200- -400 -600- -800- Reaction Progressarrow_forward
- Can u help me figure out the reaction mechanisms for these, idk where to even startarrow_forwardHi, I need your help with the drawing, please. I have attached the question along with my lab instructions. Please use the reaction from the lab only, as we are not allowed to use outside sources. Thank you!arrow_forwardHi, I need your help i dont know which one to draw please. I’ve attached the question along with my lab instructions. Please use the reaction from the lab only, as we are not allowed to use outside sources. Thank you!arrow_forward
- 5. Write the formation reaction of the following complex compounds from the following reactants: 6. AgNO₃ + K₂CrO₂ + NH₄OH → 7. HgNO₃ + excess KI → 8. Al(NO₃)₃ + excess NaOH →arrow_forwardIndicate whether the product formed in the reaction exhibits tautomerism. If so, draw the structure of the tautomers. CO₂C2H5 + CH3-NH-NH,arrow_forwardDraw the major product of this reaction N-(cyclohex-1-en-1-yl)-1-(pyrrolidino) reacts with CH2=CHCHO, heat, H3O+arrow_forward
ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
ChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill Education
Principles of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill Education
Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning
Elementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY