(a)
Interpretation:
The water (
Concept introduction:
Boiling points: The every chemical compounds is the particular temperature at which its liquid from becomes a gas or (vaporizes). For a compound to vaporize, the forces that hold the individual molecules close to each other in the liquid must be overcome.
Than the boiling point of a each compound depends on the strength of the attractive forces between the individual molecules. If the molecules are held together by strong force then a great deal of energy will be need to pull the molecules away from each other and the compound will have a high boiling point.
On the other hand, if the molecules are held together by weak forces only a small of energy be need to pull the molecules away from each other and the compound will have a low boiling point.
Dipole interaction: The boiling points of all organic molecules like (ether,
(b)
Interpretation:
The water (H2O) molecule has higher boiling point when compare to other molecules of given in the statement why, this comparison must be explain in each statements.
Concept introduction:
Boiling points: The every chemical compounds is the particular temperature at which its liquid from becomes a gas or (vaporizes). For a compound to vaporize, the forces that hold the individual molecules close to each other in the liquid must be overcome.
Than the boiling point of a each compound depends on the strength of the attractive forces between the individual molecules. If the molecules are held together by strong force then a great deal of energy will be need to pull the molecules away from each other and the compound will have a high boiling point.
On the other hand, if the molecules are held together by weak forces only a small of energy be need to pull the molecules away from each other and the compound will have a low boiling point.
Dipole interaction: The boiling points of all organic molecules like (ether, alkyl halide, amines, alcohols) also increase molecular weight because in the London dispersion forces. The boling points of these compounds, however are also affected the polar (C-Z) bonds here (Z
(c)
Interpretation:
The water (H2O) molecule has higher boiling point when compare to other molecules of given in the statement why, this comparison must be explain in each statements.
Concept introduction:
Boiling points: The every chemical compounds is the particular temperature at which its liquid from becomes a gas or (vaporizes). For a compound to vaporize, the forces that hold the individual molecules close to each other in the liquid must be overcome.
Than the boiling point of a each compound depends on the strength of the attractive forces between the individual molecules. If the molecules are held together by strong force then a great deal of energy will be need to pull the molecules away from each other and the compound will have a high boiling point.
On the other hand, if the molecules are held together by weak forces only a small of energy be need to pull the molecules away from each other and the compound will have a low boiling point.
Dipole interaction: The boiling points of all organic molecules like (ether, alkyl halide, amines, alcohols) also increase molecular weight because in the London dispersion forces. The boling points of these compounds, however are also affected the polar (C-Z) bonds here (Z= N, O, F, Cl). Generally alcohols have higher boiling point when compare to other organic molecules, because addition of London dispersion forces and the dipole-dipole interaction of the polar C-O bond, alcohol can from hydrogen bonds.
d)
Interpretation:
The H-F molecule has higher boiling point when compare to other molecules of given in the statement why, this comparison must be explain in each statements.
Concept introduction:
Boiling points: The every chemical compounds is the particular temperature at which its liquid from becomes a gas or (vaporizes). For a compound to vaporize, the forces that hold the individual molecules close to each other in the liquid must be overcome.
Than the boiling point of a each compound depends on the strength of the attractive forces between the individual molecules. If the molecules are held together by strong force then a great deal of energy will be need to pull the molecules away from each other and the compound will have a high boiling point.
On the other hand, if the molecules are held together by weak forces only a small of energy be need to pull the molecules away from each other and the compound will have a low boiling point.
Dipole interaction: The boiling points of all organic molecules like (ether, alkyl halide, amines, alcohols) also increase molecular weight because in the London dispersion forces. The boling points of these compounds, however are also affected the polar (C-Z) bonds here (Z= N, O, F, Cl). Generally alcohols have higher boiling point when compare to other organic molecules, because addition of London dispersion forces and the dipole-dipole interaction of the polar C-O bond, alcohol can from hydrogen bonds.

Trending nowThis is a popular solution!

Chapter 3 Solutions
EBK ORGANIC CHEMISTRY
- Predict the major products of the following organic reaction: O O + A ? Some important notes: • Draw the major product, or products, of the reaction in the drawing area below. • If there aren't any products, because no reaction will take place, check the box below the drawing area instead. • Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers. Explanation Check Click and drag to start drawing a structure. eserved. Terms of Use | Privacy Center >arrow_forward(EXM 2, PRBLM 3) Here is this problem, can you explain it to me and show how its done. Thank you I need to see the work for like prbl solving.arrow_forwardcan someone draw out the reaction mechanism for this reaction showing all bonds, intermediates and side products Comment on the general features of the 1H-NMR spectrum of isoamyl ester provided belowarrow_forward
- What would be the best choices for the missing reagents 1 and 3 in this synthesis? 1. PPh3 3 2. n-BuLi • Draw the missing reagents in the drawing area below. You can draw them in any arrangement you like. • Do not draw the missing reagent 2. If you draw 1 correctly, we'll know what it is. • Note: if one of your reagents needs to contain a halogen, use bromine. Click and drag to start drawing a structure.arrow_forwardIdentify the missing organic reactants in the following reaction: X + Y H+ two steps Note: This chemical equation only focuses on the important organic molecules in the reaction. Additional inorganic or small-molecule reactants or products (like H2O) are not shown. In the drawing area below, draw the skeletal ("line") structures of the missing organic reactants X and Y. You may draw the structures in any arrangement that you like, so long as they aren't touching. Click and drag to start drawing a structure. Х :arrow_forwardDraw the mechanism of friedel-crafts acylation using acetyl chloride of m-Xylenearrow_forward
- Don't used hand raiting and don't used Ai solution and correct answerarrow_forwardH R Part: 1/2 :CI: is a/an electrophile Part 2 of 2 Draw the skeletal structure of the product(s) for the Lewis acid-base reaction. Include lone pairs and formal charges (if applicable) on the structures. 4-7: H ö- H Skip Part Check X :C1: $ % L Fi Click and drag to start drawing a structure. MacBook Pro & ㅁ x G 0: P Add or increase positive formal cha Save For Later Submit ©2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centearrow_forwardDraw the friedel-crafts acylation mechanism of m-Xylenearrow_forward
- Chemistry by OpenStax (2015-05-04)ChemistryISBN:9781938168390Author:Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark BlaserPublisher:OpenStaxChemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning

