Concept explainers
(a)
Interpretation:
Given ionic species has to be drawn; mechanism for the conversion 3 to 4 has to be drawn.
Concept Introduction:
Reaction of Grignard reagent with reactant: Grignard reagent acts as strong base and deprotonate the polar reactant by capturing proton forming Hydrocarbon.
Ionic species: The bond formed between two atoms becomes ionic when large electronegative difference exists. An ionic bond is formed from the transfer of an electron from a metal atom to a non-metal atom. Ionic bonds involve a cation and anion which held by electrostatic force of attraction.
Electronegativity Difference, ΔE | Polarity | Bond Type |
ΔE = 0.00 | nonpolar | pure covalent |
0.00 < ΔE < 0.65 | nonpolar | covalent |
0.65 < ΔE < 1.67 | polar | covalent |
1.67 < ΔE | ionic |
(b)
Interpretation:
The location of C-D signal in the spectrum has to be identified and explained.
Concept Introduction:
Hooke’s law: Law enables to approximate the frequency of vibration for a bond between two masses. Generally, bond stretching is dependent on two factors: bond strength and masses of the atoms sharing the bond.
Where, f indicate force constant (bond strength)
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Chapter 3 Solutions
ORGANIC CHEMISTRYPKGDRL+MLCRL MDL
- Which of the following molecules are NOT typical carbohydrates? For the molecules that are carbohydrates, label them as an aldose or ketose. HO Он ОН ОН Он ОН но ΤΗ HO ОН HO eve Он он ОН ОН ОН If polyethylene has an average molecular weight of 25,000 g/mol, how many repeat units are present?arrow_forwardDraw the a-anomer cyclized pyranose Haworth projection of the below hexose. Circle the anomeric carbons. Number the carbons on the Fischer and Haworth projections. Assign R and S for each chiral center. HO CHO -H HO -H H- -OH H -OH CH₂OH Draw the ẞ-anomer cyclized furanose Haworth projection for the below hexose. Circle the anomeric carbons. Number the carbons on the Fischer and Haworth projections. HO CHO -H H -OH HO -H H -OH CH₂OHarrow_forwardName the below disaccharide. Circle any hemiacetals. Identify the numbering of glycosidic linkage, and identify it as a or ẞ. OH HO HO OH HO HO HO OHarrow_forward
- What are the monomers used to make the following polymers? F. а. b. с. d. Вецер хочому なarrow_forward1. Propose a reasonable mechanism for the following transformation. I'm looking for curved mechanistic arrows and appropriate formal charges on intermediates. OMe MeO OMe Me2N NMe2 OTBS OH xylenes OMe 'OTBSarrow_forwardWhat is the polymer made from the following monomers? What type of polymerization is used for each? а. ОН H2N но b. ن -NH2 d. H₂N NH2 довarrow_forward
- Condensation polymers are produced when monomers containing two different functional groups link together with the loss of a small molecule such as H2O. The difunctional monomer H2N(CH2)6COOH forms a condensation polymer. Draw the carbon-skeleton structure of the dimer that forms from this monomer.arrow_forwardWhat is the structure of the monomer?arrow_forward→ BINDERIYA GANBO... BINDERIYA GANBO. AP Biology Notes Gamino acid chart - G... 36:22 司 10 ☐ Mark for Review Q 1 Hide 80 8 2 =HA O=A¯ = H₂O Acid HIO HBrO HCIO Question 10 of 35 ^ Σ DELL □ 3 % Λ & 6 7 * ∞ 8 do 5 $ 4 # m 3 ° ( 9 Highlights & Notes AXC Sign out Carrow_forward
- Which representation(s) show polymer structures that are likely to result in rigid, hard materials and those that are likely to result in flexible, stretchable, soft materials?arrow_forward3. Enter the molecular weight of the product obtained from the Williamson Ether Synthesis? OH OH & OH excess CH3l Ag₂Oarrow_forwardPlease answer 1, 2 and 3 on the endarrow_forward
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