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(a)
To explain:
Type of attractive force formed in between molecule
Introduction:
London forces include the forces which are temporarily formed between non-polar hydrocarbon molecules as a result of formation of electron cloud of atoms.
Dipole-dipole interactions are formed between molecules due to formation of partial positive and negative charges on atoms due to their electronegativity differences.
Ion-dipole interactions are formed between polar molecules like water which contain partial
Ionic interactions are formed between positively charged cation and a negatively charged anion.
(b)
To explain:
Type of attractive force formed in between molecule
Introduction:
London forces include the forces which are temporarily formed between non-polar hydrocarbon molecules as a result of formation of electron cloud of atoms.
Dipole-dipole interactions are formed between molecules due to formation of partial positive and negative charges on atoms due to their electronegativity differences.
Ion-dipole interactions are formed between polar molecules like water which contain partial functional groups and charged functional groups or between small electronegative atoms.
Ionic interactions are formed between positively charged cation and a negatively charged anion.
(c)
To explain:
Type of attractive force formed in between molecule
Introduction:
London forces include the forces which are temporarily formed between non-polar hydrocarbon molecules as a result of formation of electron cloud of atoms.
Dipole-dipole interactions are formed between molecules due to formation of partial positive and negative charges on atoms due to their electronegativity differences.
Ion-dipole interactions are formed between polar molecules like water which contain partial functional groups and charged functional groups or between small electronegative atoms.
Ionic interactions are formed between positively charged cation and a negatively charged anion.
(d)
To explain:
Type of attractive force formed in between molecule
Introduction:
London forces include the forces which are temporarily formed between non-polar hydrocarbon molecules as a result of formation of electron cloud of atoms.
Dipole-dipole interactions are formed between molecules due to formation of partial positive and negative charges on atoms due to their electronegativity differences.
Ion-dipole interactions are formed between polar molecules like water which contain partial functional groups and charged functional groups or between small electronegative atoms.
Ionic interactions are formed between positively charged cation and a negatively charged anion.
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Chapter 7 Solutions
EBK LABORATORY MANUAL FOR GENERAL, ORGA
- 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
- Don't used hand raiting and don't used Ai solutionarrow_forward1. Base on this experimental results, how do you know that the product which you are turning in is methyl 3-nitrobenzoate(meta substituted product ) rather than either of the other two products? 2. What observation suggests that at least a small amount of one or both of the other two isomers are in the mother liquor?arrow_forwardExplain Huckel's rule.arrow_forward
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