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Concept explainers
(a)
Interpretation:
The systematic name given should be checked that whether it is correct or not and also the correct name should be given if in case the given name is wrong.
Concept Introduction:
NOMENCLATURE RULES:
- If the ‘ane’ ending of the
alkane is replaced by ‘yne’ ending, the name of alkyne is obtained. - Select the longest chain which contains the triple bond in such a way to get lowest value for the
functional group . - Two types of
alkynes will be there according to the position of triple bond. Terminal alkyne is the one which contain triple bond at the end of the chain and internal alkyne is the one which contain triple bond not at the end but present in any other positions in the chain. - When the counting is done from either sides of triple bond in a compound which contain same number for the functional group suffix, the correct name will be the one which have lowest substituent number. In the case of more than one substituent, alphabetical order should be followed.
Skeletal structure: When the atoms bonded in a compound is drawn in a series it can be called as a skeletal structure. In the skeletal structure, we can show the branches, chains, rings or any other hetero atom other than carbon or hydrogen.
Condensed structure: In the condensed structure, atoms or group of atoms are expressed in a line. But it does not contain any vertical bonds and also the horizontal single bonds.
(b)
Interpretation:
The systematic name given should be checked that whether it is correct or not and also the correct name should be given if in case the given name is wrong.
Concept Introduction:
NOMENCLATURE RULES:
- If the ‘ane’ ending of the alkane is replaced by ‘yne’ ending, the name of alkyne is obtained.
- Select the longest chain which contains the triple bond in such a way to get lowest value for the functional group.
- Two types of alkynes will be there according to the position of triple bond. Terminal alkyne is the one which contain triple bond at the end of the chain and internal alkyne is the one which contain triple bond not at the end but present in any other positions in the chain.
- When the counting is done from either sides of triple bond in a compound which contain same number for the functional group suffix, the correct name will be the one which have lowest substituent number. In the case of more than one substituent, alphabetical order should be followed.
Skeletal structure: When the atoms bonded in a compound is drawn in a series it can be called as a skeletal structure. In the skeletal structure, we can show the branches, chains, rings or any other hetero atom other than carbon or hydrogen.
Condensed structure: In the condensed structure, atoms or group of atoms are expressed in a line. But it does not contain any vertical bonds and also the horizontal single bonds.
(c)
Interpretation:
The systematic name given should be checked that whether it is correct or not and also the correct name should be given if in case the given name is wrong.
Concept Introduction:
NOMENCLATURE RULES:
- If the ‘ane’ ending of the alkane is replaced by ‘yne’ ending, the name of alkyne is obtained.
- Select the longest chain which contains the triple bond in such a way to get lowest value for the functional group.
- Two types of alkynes will be there according to the position of triple bond. Terminal alkyne is the one which contain triple bond at the end of the chain and internal alkyne is the one which contain triple bond not at the end but present in any other positions in the chain.
- When the counting is done from either sides of triple bond in a compound which contain same number for the functional group suffix, the correct name will be the one which have lowest substituent number. In the case of more than one substituent, alphabetical order should be followed.
Skeletal structure: When the atoms bonded in a compound is drawn in a series it can be called as a skeletal structure. In the skeletal structure, we can show the branches, chains, rings or any other hetero atom other than carbon or hydrogen.
Condensed structure: In the condensed structure, atoms or group of atoms are expressed in a line. But it does not contain any vertical bonds and also the horizontal single bonds.
(d)
Interpretation:
The systematic name given should be checked that whether it is correct or not and also the correct name should be given if in case the given name is wrong.
Concept Introduction:
NOMENCLATURE RULES:
- If the ‘ane’ ending of the alkane is replaced by ‘yne’ ending, the name of alkyne is obtained.
- Select the longest chain which contains the triple bond in such a way to get lowest value for the functional group.
- Two types of alkynes will be there according to the position of triple bond. Terminal alkyne is the one which contain triple bond at the end of the chain and internal alkyne is the one which contain triple bond not at the end but present in any other positions in the chain.
- When the counting is done from either sides of triple bond in a compound which contain same number for the functional group suffix, the correct name will be the one which have lowest substituent number. In the case of more than one substituent, alphabetical order should be followed.
Skeletal structure: When the atoms bonded in a compound is drawn in a series it can be called as a skeletal structure. In the skeletal structure, we can show the branches, chains, rings or any other hetero atom other than carbon or hydrogen.
Condensed structure: In the condensed structure, atoms or group of atoms are expressed in a line. But it does not contain any vertical bonds and also the horizontal single bonds.
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Chapter 6 Solutions
Essential Organic Chemistry Study Guide & Solution Manual, Books a la Carte Edition
- In the solid state, oxalic acid occurs as a dihydrate with the formula H2C2O4 C+2H2O. Use this formula to calculate the formula weight of oxalic acid. Use the calculated formula weight and the number of moles (0.00504mol) of oxalic acid in each titrated unknown sample recorded in Table 6.4 to calculate the number of grams of pure oxalic acid dihydrate contained in each titrated unknown sample.arrow_forward1. Consider a pair of elements with 2p and 4p valence orbitals (e.g., N and Se). Draw their (2p and 4p AO's) radial probability plots, and sketch their angular profiles. Then, consider these orbitals from the two atoms forming a homonuclear л-bond. Which element would have a stronger bond, and why? (4 points)arrow_forwardWrite the reaction and show the mechanism of the reaction. Include the mechanism for formation of the NO2+ 2. Explain, using resonance structures, why the meta isomer is formed. Draw possible resonance structures for ortho, meta and para.arrow_forward
- Nonearrow_forward3. A molecular form of "dicarbon", C2, can be generated in gas phase. Its bond dissociation energy has been determined at 599 kJ/mol. Use molecular orbital theory to explain why energy of dissociation for C₂+ is 513 kJ/mol, and that for C2² is 818 kJ/mol. (10 points)arrow_forward9.73 g of lead(IV) chloride contains enough Cl- ions to make ____ g of magnesium chloride.arrow_forward
- 6. a) C2's. Phosphorus pentafluoride PF5 belongs to D3h symmetry group. Draw the structure of the molecule, identify principal axis of rotation and perpendicular (4 points) b) assume that the principal axis of rotation is aligned with z axis, assign symmetry labels (such as a1, b2, etc.) to the following atomic orbitals of the P atom. (character table for this group is included in the Supplemental material). 3s 3pz (6 points) 3dz²arrow_forward2. Construct Lewis-dot structures, and draw VESPR models for the ions listed below. a) SiF5 (4 points) b) IOF4 (4 points)arrow_forward5. Complex anion [AuCl2]¯ belongs to Doh symmetry point group. What is the shape of this ion? (4 points)arrow_forward
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