Chapter 1: 18P (page 76)
Predict the hybridization, geometry, and bond angles for the carbon and nitrogen atoms in acetonitriles
Short Answer
Answer | Hybridization |
2 | sp |
3 | sp2 |
4 | sp3 |
Chapter 1: 18P (page 76)
Predict the hybridization, geometry, and bond angles for the carbon and nitrogen atoms in acetonitriles
Answer | Hybridization |
2 | sp |
3 | sp2 |
4 | sp3 |
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Get started for freeQuestion: Use electronegativities to predict the direction of the dipole moments of the following bonds.
Give the relationship between the following pairs of structures. The relationships are:
Same compound
Constitutional isomers (structural isomers)
Cis-trans isomers
Not isomers (different molecular formula)
Question: For each of the following compounds, draw the important resonance forms. Indicate which structures are major and minor contributors or whether they have the same energy.
A. H2CNN
Question: Compound X, isolated from lanolin (sheep’s wool fat), has the pungent aroma of dirty sweat socks. A careful analysis showed that compound Xcontains 62.0%carbon and 10.4%hydrogen. No nitrogen or halogen was found.
(a) Compute an empirical formula for compound X.
(b) A molecular weight determination showed that compound Xhas a molecular weight of approximately 117. Find the molecular formula of compound X.
(c) Many possible structures have this molecular formula. Draw complete structural formulas for four of them.
Compute the empirical and molecular formulas for each of the following elemental analyses. In each case, propose at least one structure that fits the molecular formula.
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