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Concept explainers
(a)
Interpretation:
The systematic name for each isomer has to be given.
Concept introduction:
The many of 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 in major namely Prefix, suffix and root word.
The bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, rather the bonds in between carbon atoms and to the hetero atoms are drawn as line segments. For acyclic, linear carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon. For representing a heteroatom attached to the carbon, use a line segment and label the heteroatom at the end of their line segment.
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.
Nomenclature of organic molecules: The particular functional group connected into a primary carbon atom, while secondary and tertiary groups in (C2 and C3) place of carbon atoms it is called primary, secondary and tertiary structures.
(b)
Interpretation:
The common name for each isomer has to be given.
Concept introduction:
The many of 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 in major namely Prefix, suffix and root word.
The bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, rather the bonds in between carbon atoms and to the hetero atoms are drawn as line segments. For acyclic, linear carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon. For representing a heteroatom attached to the carbon, use a line segment and label the heteroatom at the end of their line segment.
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. For example alkynes molecules, suffix will be ‘yne’.
Root word represents the longest continuous carbon skeleton of the organic molecule.
Nomenclature of organic molecules: The particular functional group connected into a primary carbon atom, while secondary and tertiary groups in (C2 and C3) place of carbon atoms it is called primary, secondary and tertiary structures.
(c)
Interpretation:
The number of primary
Concept introduction:
The many of 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 in major namely Prefix, suffix and root word.
The bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, rather the bonds in between carbon atoms and to the hetero atoms are drawn as line segments. For acyclic, linear carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon. For representing a heteroatom attached to the carbon, use a line segment and label the heteroatom at the end of their line segment.
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. For example alkynes molecules, suffix will be ‘yne’.
Root word represents the longest continuous carbon skeleton of the organic molecule.
Nomenclature of organic molecules: The particular functional group connected into a primary carbon atom, while secondary and tertiary groups in (C2 and C3) place of carbon atoms it is called primary, secondary and tertiary structures.
(d)
Interpretation:
The number of secondary alkyl halide has to be given.
Concept introduction:
The many of 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 in major namely Prefix, suffix and root word.
The bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, rather the bonds in between carbon atoms and to the hetero atoms are drawn as line segments. For acyclic, linear carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon. For representing a heteroatom attached to the carbon, use a line segment and label the heteroatom at the end of their line segment.
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. For example alkynes molecules, suffix will be ‘yne’.
Root word represents the longest continuous carbon skeleton of the organic molecule.
Nomenclature of organic molecules: The particular functional group connected into a primary carbon atom, while secondary and tertiary groups in (C2 and C3) place of carbon atoms it is called primary, secondary and tertiary structures.
(e)
Interpretation:
The number of tertiary alkyl halide has to be given.
Concept introduction:
The many of 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 in major namely Prefix, suffix and root word.
The bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, rather the bonds in between carbon atoms and to the hetero atoms are drawn as line segments. For acyclic, linear carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon. For representing a heteroatom attached to the carbon, use a line segment and label the heteroatom at the end of their line segment.
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. For example alkynes molecules, suffix will be ‘yne’.
Root word represents the longest continuous carbon skeleton of the organic molecule.
Nomenclature of organic molecules: The particular functional group connected into a primary carbon atom, while secondary and tertiary groups in (C2 and C3) place of carbon atoms it is called primary, secondary and tertiary structures.
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Chapter 3 Solutions
EBK ORGANIC CHEMISTRY
- Question 2 0/1 pts Provide the proper IUPAC name only for the following compound. Dashes, commas, and spaces must be used correctly. HO CH 3 1-methyl-1-cyclohexanecarboxylic acidarrow_forwardPlease assign all the carbons for C-NMR and hydrogen for H-NMR. Please if I can get that less than hourarrow_forwardAssign these peaks spectrum ( H-NMR and C-NMR)arrow_forward
- 3. For the following reaction, what are the major product(s) mechanism for this reaction ? and draw the full Br Brarrow_forward4. Show the product(s) for the following reaction if it proceeds via the S42 mechanism AND if it proceeds via an Syt mechanism? Draw the mechanisms for both reactions and show all resonance structures for any intermediates. Would you expect the Su or Sy2 reaction to be favoured and why? NGOarrow_forwardI have a question here so in essence were just comparing the electronegativity values that are being given, soC and Cl, C and O, C and H to determine the partially positive, partially negative charges? So option I: Cl and C, option 2 O and C, option III C on its own correct?arrow_forward
- Draw the less stable chair conformation of myo-inositol clearly indicating the axial and equatorial substituents as well as the cis and trans relationships of at least 3 OH groups. Draw a viable Newman Projection using any carbon carbon bond clearly showing a gauche interaction between the substituents.arrow_forward5. What is the product for the following reaction for each step and draw the mechanism H 1. NaNH2 2, EtBrarrow_forwardmical lation or mula trations, AAAAAAAAAAAAA Experiment #8 Electrical conductivity & Electrolytes Conductivity of solutions FLINN Scientific conductivity meter scale - RED LED Scale 0 Green LED OFF OFF 1 Dim OFF 2 medium OFF Bright Dim 4 Very Bright Medium 3 LED Conductivity Low or None' Low Medium High very high SE = Strong Electrolyte, FE = Fair Electrolyte WE Weak Electrolyte, NE= Noni Electrolyte 9 0.1 M NaOH. 10. 0.1M NH3 11. D.1M HCT 12. 0.1 M HC2H3D2 13 0 m H2SO4 Prediction observed conductivity ? Very bright red, dim green (4) ? Saturated Bright red, dim green 3 Cacal) Bright red, dim green 3 Prediction Bright red, No green ? observed Bright red,dim green ? Conductivity Just red? I Can you help me understand how I'm supposed to find the predictions of the following solutions? I know this is an Ionic compound and that the more ions in a solution means it is able to carry a charge, right? AAAAAA The light are not matching up with the scale So I'm confused about what I should be…arrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage Learning
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage LearningWorld of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage Learning
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