Concept explainers
(a)
Interpretation:
The structure with systematic name of the products has to be drawn when adding
Concept Introduction:
Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry).IUPAC name consists of three parts, namely Prefix, suffix and root word.
Prefix- Represents the substituent present in the molecule and its position in the root name.
Suffix- Denotes the presence of
Root word - Represents the longest continuous carbon skeleton of the organic molecule.
Markovnikov’s rule: unsymmetrical alkene reacts with hydrogen halide, halide ions goes to the more substitution position of carbon-carbon double bond which provides
(b)
Interpretation:
The structure with systematic name of the products has to be drawn when adding
Concept Introduction:
Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry).IUPAC name consists of three parts, namely Prefix, suffix and root word.
Prefix- Represents the substituent present in the molecule and its position in the root name.
Suffix- Denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc. To add suffix to name a compound, the suffix “-ane” in the parent alkane is replaced by the respective suffix, which corresponds to the functional group present in the given compound. For carboxylic acid, suffix “-oic” will be added, for alcohol, suffix “-ol” will be added and so on
Root word - Represents the longest continuous carbon skeleton of the organic molecule.
Markovnikov’s rule: unsymmetrical alkene reacts with hydrogen halide, halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.
(c)
Interpretation:
The structure with systematic name of the products has to be drawn when adding
Concept Introduction:
Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry).IUPAC name consists of three parts, namely Prefix, suffix and root word.
Prefix- Represents the substituent present in the molecule and its position in the root name.
Suffix- Denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc. To add suffix to name a compound, the suffix “-ane” in the parent alkane is replaced by the respective suffix, which corresponds to the functional group present in the given compound. For carboxylic acid, suffix “-oic” will be added, for alcohol, suffix “-ol” will be added and so on
Root word - Represents the longest continuous carbon skeleton of the organic molecule.
Markovnikov’s rule: unsymmetrical alkene reacts with hydrogen halide, halide ions goes to the more substitution position of carbon-carbon double bond which provides alkyl halides.
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Chapter 23 Solutions
Chemistry and Chemical Reactivity - AP Edition
- 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
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning
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