![Organic Chemistry](https://www.bartleby.com/isbn_cover_images/9781305580350/9781305580350_largeCoverImage.gif)
Concept explainers
(a)
Interpretation:
The solvent with greater solubility in water has to be selected.
Concept Introduction:
Hydrogen bonding: The attractive interactions between hydrogen atom bonded to an atom of high electronegativity (most commonly O or N) and a lone pair of electrons on another atom of electrons on another atom of high electronegativity (again, most commonly O or N).
Solubility: Interaction of polar compound with water occurs by hydrogen bonding formation between compounds and water.
Hydrogen-bond donors: The hydrogen atom that is attached to the high electronegative atom participates in hydrogen bond. Thus, that Hydrogen atom is known as hydrogen-bond donors.
Hydrogen-bond acceptor: The atom (high electronegative atom with lone pairs) to which the hydrogen atom is participated in hydrogen bond.
(b)
Interpretation:
The solvent with greater solubility in water has to be selected.
Concept Introduction:
Hydrogen bonding: The attractive interactions between hydrogen atom bonded to an atom of high electronegativity (most commonly O or N) and a lone pair of electrons on another atom of electrons on another atom of high electronegativity (again, most commonly O or N).
Solubility: Interaction of polar compound with water occurs by hydrogen bonding formation between compounds and water.
Hydrogen-bond donors: The hydrogen atom that is attached to the high electronegative atom participates in hydrogen bond. Thus, that Hydrogen atom is known as hydrogen-bond donors.
Hydrogen-bond acceptor: The atom (high electronegative atom with lone pairs) to which the hydrogen atom is participated in hydrogen bond.
(c)
Interpretation:
The solvent with greater solubility in water has to be selected.
Concept Introduction:
Hydrogen bonding: The attractive interactions between hydrogen atom bonded to an atom of high electronegativity (most commonly O or N) and a lone pair of electrons on another atom of electrons on another atom of high electronegativity (again, most commonly O or N).
Solubility: Interaction of polar compound with water occurs by hydrogen bonding formation between compounds and water.
Hydrogen-bond donors: The hydrogen atom that is attached to the high electronegative atom participates in hydrogen bond. Thus, that Hydrogen atom is known as hydrogen-bond donors.
Hydrogen-bond acceptor: The atom (high electronegative atom with lone pairs) to which the hydrogen atom is participated in hydrogen bond.
(d)
Interpretation:
The solvent with greater solubility in water has to be selected.
Concept Introduction:
Hydrogen bonding: The attractive interactions between hydrogen atom bonded to an atom of high electronegativity (most commonly O or N) and a lone pair of electrons on another atom of electrons on another atom of high electronegativity (again, most commonly O or N).
Solubility: Interaction of polar compound with water occurs by hydrogen bonding formation between compounds and water.
Hydrogen-bond donors: The hydrogen atom that is attached to the high electronegative atom participates in hydrogen bond. Thus, that Hydrogen atom is known as hydrogen-bond donors.
Hydrogen-bond acceptor: The atom (high electronegative atom with lone pairs) to which the hydrogen atom is participated in hydrogen bond.
![Check Mark](/static/check-mark.png)
Want to see the full answer?
Check out a sample textbook solution![Blurred answer](/static/blurred-answer.jpg)
Chapter 10 Solutions
Organic Chemistry
- Arrange these compounds in order of increasing boiling point (values in °C are -42, -24, 78, and 118). (a) CH,CH,OH (b) CH,OCH, (c) CH,CH,CH, (d) CH,COOHarrow_forwardDescribe concisely a chemical test to distinguish between the following pairs of compounds.(a) Propanal and propanone(b) Phenol and benzoic acid(c) Hexan-3-one and hexan-2-onearrow_forwardGive reasons for the following :(i) Phenol is more acidic than methanol.(ii) The C—O—H bond angle in alcohols is slightly less than the tetrahedral angle (190°28′).(iii) (CH3)3C—O—CH3 on reaction with HI gives (CH3)3C—I and CH3—OH as the main products and not (CH3)3C—OH and CH3—I.arrow_forward
- Phenylethanol can be oxidised to phenylethanal or phenylethanoic acid, depending on the reagents used (both the alcohol and the aldehyde are of interest for their antimicrobial properties, while the acid is used to treat type II hyperammonemia): A (a) (b) (c) CoH,CH,CHO phenylethanal B C6H5CH₂CH₂OHC₂H₂CH₂CO₂H phenylethanol Suggest reagents (shown as A and B in the scheme above) that could be used to carry out the oxidation of the alcohol to the aldehyde and the acid, respectively. C6H5CH₂- Suggest two other syntheses of phenylethanoic acid, in each case indicating the starting materials and other reagents required, but not giving details of mechanism. One of your proposed syntheses must start with a compound which only contains seven carbon atoms (the acid product contains eight carbon atoms). phenylethanoic acid Phenylethanal can be converted to a hydrate in the presence of aqueous acid, though the position of equilibrium is very far to the left: H H+/H₂O OH C6H5CH₂-C-H OH Explain why…arrow_forwardProvide the IUPAC name for each of the following compounds. Pay attention to stereochemistry. (c) (a) (Б) О NO2 OH NH2 ОН NH2arrow_forward6. Describe concisely a chemical test to distinguish between the following pairs of compounds. (a) n-pentanol and 3-methylpentan-3-ol (b) Ethanal dan pentanal (c) Phenol and benzoic acidarrow_forward
- Explain a procedure to separate a mixture of the following 3 compounds to 3 separate individual components. May use any organic solvents and reagents. (Part A is first mixture, Part B is second mixture) First answer (a) then (b)arrow_forwardWrite the reagent or draw structures of the starting material or organic product(s) in the following reactions. If more than one product is formed, identify the major product where possible. (a) (b) HO OH OH H2SO4 ? Cl₂ ? FeCl3arrow_forwardName the following carboxylic acid derivatives, giving both a common name and anIUPAC name where possible.(a) PhCOOCH2CH(CH3)2arrow_forward
- Answer the following problem and show your complete explanation for better understanding. READ THE PROBLEM. COMMON NAME AND IUPAC NAMEarrow_forwardAssume that you have samples of the following two compounds, both with formula C7H8O. Both compounds dissolve in ether, but only one of the two dissolves in aqueous NaOH. How could you use this information to distinguish between them?arrow_forwardWhich of the following pure compounds can form hydrogen bonds? Which can form hydrogen bonds with water? Which ones do you expect to be soluble in water?(a) (CH3CH2)2NH (b) (CH3CH2)3N (c) CH3CH2CH2OHarrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples 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 EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305957404/9781305957404_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781259911156/9781259911156_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305577213/9781305577213_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9780078021558/9780078021558_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305079373/9781305079373_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781118431221/9781118431221_smallCoverImage.gif)