(a)
Interpretation:
The configuration of the given structure of citric acid has to be determined.
Concept introduction:
According to Cahn-Ingold-Prelog system,
The group attached to asymmetric center should be ranked based on the
Check the direction of arrow drawn in the direction of decreasing priority. If the arrow points clockwise direction, then the compound has R configuration. If the arrow points counterclockwise direction, then the compound has S configuration. If the group with lowest priority is not bonded by a hatched wedge, then interchange this group (lowest priority) by group bonded to hatched wedge and draw the arrow in priority order but the configuration is assigned as just reverse.
(b)
Interpretation:
The chirality of citric acid if
Concept introduction:
Optical activity of a molecule is the interaction between molecule and plane-polarized light.
Molecule having asymmetric center shows optical activity except mesocompounds.
Asymmetric center is a stereocenter which arises to hydrocarbons if the carbon is bonded to four different groups.
Want to see the full answer?
Check out a sample textbook solutionChapter 4 Solutions
EP ESSENTIAL ORG.CHEM.-MOD.MASTERING
- When ethylamine, a weak base (Kb=4.3104) , reacts with formic acid, a weak acid (Ka=1.8104) , the following reaction takes place: CH3CH2NH2(aq)+HCOOH(aq)CH3CH2NH3+(aq)+HCOO(aq) Calculate K for this reaction.arrow_forwardCatalytic cracking is an industrial process used to convert high-molecular-weight hydrocarbons to low-molecular-weight hydrocarbons. A petroleum company has a huge supply of heating oil stored as straight-chain C17H36, and demand has picked up for shorter chain hydrocarbons to be used in formulating gasoline. The company uses catalytic cracking to create the shorter chains necessary for gasoline. If they produce two molecules in the cracking, and 1-octene is one of them, what is the formula of the other molecule produced? As part of your answer, draw the condensed structural formula of the 1-octene.arrow_forwardCertain omega-3 fatty acids can be found only in animal sources, such as fatty fish. Two of these are eicosapentaenoic acid (EPA) [20:5] and docosahexaenoic acid (DHA) [22:6], both of which are ω-3 fatty acids. DHA has been shown to be important in healthy brain development, so it has recently been added to infant formulas. Breast milk is rich in DHA as long as the mother maintains a healthy diet that includes fish. Draw skeletal structures of the fatty acids EPA and DHA.arrow_forward
- 2-Butanone is reduced by hydride ion donors, such assodium borohydride (NaBH₄), to the alcohol 2-butanol. Eventhough the alcohol has a chiral center, the product isolated from the redox reaction is not optically active. Explain.arrow_forwardCortisone is a compound that is used as an anti-inflammatory drug to treat 2) diseases like arthritis. Cortisone is a steroid which contains four rings (A, B, C and D), and has the following structure: он "OH Cortisone Provide the data to complete each of the following statements: The total number of chiral carbons (stereocentres) in Cortisone is The maximum number of stereoisomers possible is: The degree of unsaturation (IHD) of Cortisone is The total number of 2° hydrogens is The ring fusion between rings B and C is trans or cis? The absolute configuration of the carbon with * in the structure is The total number of n bonds isarrow_forwardAlkenes can be converted to alcohols by reaction with mercuric acetate to form a β-hydroxyalkylmercury(II) acetate compound, a reaction called oxymercuration. Subsequent reduction with NaBH4 reduces the C–Hg bond to a C–H bond, forming the alkyl alcohol, a reaction called demercuration. Draw the structures of the Hg-containing compound(s) and the final alcohol product(s) formed in the following reaction sequence, omitting byproducts. If applicable, draw hydrogen at a chirality center and indicate stereochemistry via wedge-and-dash bonds.arrow_forward
- Alkenes can be converted to alcohols by reaction with mercuric acetate to form a β-hydroxyalkylmercury(II) acetate compound, a reaction called oxymercuration. Subsequent reduction with NaBH4 reduces the C–Hg bond to a C–H bond, forming the alkyl alcohol, a reaction called demercuration. Draw the structures of the Hg-containing compound(s) and the final alcohol product(s) formed in the following reaction sequence, omitting byproducts. If applicable, draw hydrogen at a chirality center and indicate stereochemistry via wedge-and-dash bonds.arrow_forwardGiven the reaction: benzoyl chloride + acetic acid Draw the structure of the tetrahedral intermediate that is formed and indicate how it dissociates to give the reaction product (use arrows).arrow_forward2. Sucrose is a disaccharide formed from the condensation of glucose and fructose sugars. Draw the structure of sucrose that results from the condensation reaction between the indicated -OH groups. CH2OH 1, CH,OH он 1. OH но CH,OH OH HO H он OHarrow_forward
- Xylulose has the following structural formula. To what carbohydrate class does xylulose belong based on the number of carbons and carbonyl functionality? A) aldotetrose B) aldopentose C) ketotetrose D) ketopentose E) ketohexosearrow_forwardDraw the condensed structural formulas for the products of the following: CH3−CH2−NH2+HCl⟶arrow_forwardCount the number of chiral carbons in the given compounds and assign each chiral carbon as R or Sarrow_forward
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningChemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub CoOrganic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage LearningIntroduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage LearningChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage Learning