Concept explainers
(a)
Interpretation:
The approximate value for the
Concept introduction:
Hybridization is the mixing of valence atomic orbitals to get equivalent hybridized orbitals that having similar characteristics and energy.
Geometry of a molecule can be predicted by knowing its hybridization.
(b)
Interpretation:
The bond angles for the four
Concept introduction:
Hybridization is the mixing of valence atomic orbitals to get equivalent hybridized orbitals that having similar characteristics and energy.
Geometry of a molecule can be predicted by knowing its hybridization.
(c)
Interpretation:
The chiral carbon in the molecule has to be determined
Concept introduction:
A chiral carbon is the carbon atom which is substituted to four different groups. Due to presence of chiral carbon a molecule become chiral and it gives optical isomers also that is
All the substituents are different hence is is a chiral carbon and so molecule.
(d)
Interpretation:
The shortest bond in the molecule has to be determined
Concept introduction:
Bond order: It is the measure of number of electron pairs shared between two atoms.
Bond length is inversely proportional to the bond order.
A higher bond order results in a shorter bond for a given pair of atoms.
(e)
Interpretation:
The
Concept introduction:
A chiral carbon is the carbon atom which is substituted to four different groups. Due to presence of chiral carbon a molecule become chiral and it gives optical isomers also that is
All the substituents are different hence is is a chiral carbon and so molecule.
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Chapter 23 Solutions
Chemistry & Chemical Reactivity
- Formamide, HC(O)NH2, is prepared at high pressures from carbon monoxide and ammonia, and serves as an industrial solvent (the parentheses around the O indicate that it is bonded only to the carbon atom and that the carbon atom is also bonded to the H and the N atoms). Two resonance forms (one with formal charges) can be written for formamide. Write both resonance structures, and predict the bond angles about the carbon and nitrogen atoms for each resonance form. Are they the same? Describe how the experimental determination of the HNH bond angle could be used to indicate which resonance form is more important.arrow_forwardDraw the shape of the PFs molecule and answer the following questions: (i) What is the principal rotation axis of the PFs molecule? (ii) Does the molecule have other rotation axes? If so, what are the other rotation axes of the molecule? (iii) Does the molecule have improper rotation axes? If so, what is the improper rotation axis of the molecule? (iv) Does the molecule have ơ, mirror plane(s)? If so, how many? (v) Does the molecule have ơy mirror plane(s)? If so, how many? (vi) Does the molecule have ơa mirror plane (s)? If so, how many? (vii) What is the point group of the PF, molecule? (viii) What is the order of the point group of the PFs molecule? (ix) Using symmetry criteria, predict if the PFs molecule is polar or non-polar. (x) Using symmetry criteria, predict if the PFs molecule is chiral or non-chiral.arrow_forwardthx!arrow_forward
- CTQ 7: Why is it incorrect to describe the process of boiling as 2H,0(1) → 2H,(g) + 0,(g)?arrow_forwardDraw the shapes of the following molecules and ions in 3-dimension. Show clearly any lone pairs of electrons on the central atom, state the number of bond pairs and lone pairs of electrons on the central atom and name the shape of the molecule or ion. (a) CH3+, methyl carbocation (b) HOBr, bromic (I) acid (c) NCl3, nitrogen trichloride Provide everything stated in the instructions for each compound.arrow_forwardYeni Metin Belgesi - Not Defteri Dosya Düzen Biçim Görünüm Yardım For acetaldehyde (CH3CHO) write the Lewis structure. Write the hybridization and geometry of each carbon. Draw its 3D structure and write the bond angles (approximately).arrow_forward
- For the following descriptions of molecules, draw the Lewis structure (showing all atoms, lone pairs, formal charges) of the molecule and show all bond angles (assuming ideal VSEPR angles). An organic compound with the molecular formula H3CNO2. C is sp2 hybridized, N is sp3 hybridized, one O is sp² hybridized, while the second O is sp3 hybridized. An organic compound with the molecular formula H2CNO*. Both C and O are sp hybridized while N is sp³ hybridized.arrow_forwardIn the following compounds, the C atoms form a single ring.Draw a Lewis structure for each compound, identify cases for which resonance exists, and determine the carbon-carbon bondorder(s): (a) C₃H₄; (b) C₃H₆; (c) C₄H₆; (d) C₄H₄; (e) C₆H₆.arrow_forwardButadiene, C4H6, is a planar molecule that has the followingcarbon–carbon bond lengths: (a) Predict the bond angles around each of the carbon atoms and sketch the molecule. (b) From left to right, what is the hybridization of each carbon atom in butadiene? (c) The middle C—C bond length in butadiene (1.48 Å) is a little shorter than the average C—C single bond length (1.54 Å). Does this imply that the middle C—C bond in butadiene is weaker or stronger than the average C—C single bond? (d) Based on your answer for part (c), discuss what additional aspects of bonding in butadiene might support the shorter middle C—C bond.arrow_forward
- Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage LearningChemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning