Concept explainers
(a)
Interpretation:
Lewis structure of
Concept Introduction:
Lewis structures represent covalent bonds and describe valence electrons configuration of atoms. The covalent bonds are depicted by lines and unshared electron pairs by pairs of dots. The sequence to write Lewis structure of some molecule is given as follows:
- The central atom is identified and various other atoms are arranged around it. This central atom so chosen is often the least electronegative.
- Total valence electrons are estimated for each atom.
- single bond is first placed between each atom pair.
- The electrons left can be allocated as unshared electron pairs or as multiple bonds around the
symbol of the element to satisfy the octet (or duplet) for each atom. - Add charge on the overall structure in case of polyatomic cation or anion.
(a)

Explanation of Solution
Hence, 6 pairs are to be allocated to form the Lewis structure of
Similarly, total valence electrons is sum of the valence electrons for each atom along with a charge in
Hence, 8 pairs are to be allocated to form the Lewis structure of
Likewise, total valence electrons in
Hence, 10 pairs are to be allocated to form the Lewis structure of
(b)
Interpretation:
The hybridization at each carbon in
Concept Introduction:
The table that relates the steric number with hybridization is as follows:
(b)

Explanation of Solution
In the structure of
The terminal carbon atoms at positions 1 and 2 are trigonal planar with 3 as steric number hence the hybridization of these carbon atoms is
In the structure of
Since the steric number around central carbon is 2 therefore, the hybridization of carbon atom located at positions 2 is
In the structure of
Central carbon atoms have effectively two bond pairs as each double bond is regarded as one single bond pair. Since the steric number around central carbon atoms is 2 therefore, the hybridization of carbon atoms located at positions 2 and 3 is
The terminal carbon atoms at positions 1 and 4 are trigonal planar with 3 as steric number hence the hybridization of this carbon is
(c)
Interpretation:
The type of bonds that connect carbon atoms in
Concept Introduction:
A single bond is always associated with sigma bonds. Molecules that have all atoms connected by sigma bond exclusively are stated to be in
A double bond and carbocation are associated with
A triple bond or central carbon structure similar to allene is always associated with
(c)

Explanation of Solution
In
In
In
(d)
Interpretation:
The bond angles in
Concept Introduction:
Refer to part (c).
(d)

Explanation of Solution
A single bond is always associated with sigma bonds. Molecules that have all atoms connected by sigma bond exclusively are stated to be in
A double bond and carbocation are associated with
A triple bond or central carbon structure similar to allene is always associated with
Thus the bond angles can be illustrated as follows:
(e)
Interpretation:
Whether all hydrogen atoms lie in the same plane or not in
Concept Introduction:
Refer to part (c).
(e)

Explanation of Solution
In allene, the central carbon that is double bonded to each carbon in different planes is
Thus the terminal hydrogen atom on carbon at position 1 is in a different plane than carbon at position 3 in case of
(f)
Interpretation:
Orientation of hydrogen atoms at end of chain has to be determined.
Concept Introduction:
In allene, the central carbon that is double bonded to each carbon in different planes is
(f)

Explanation of Solution
For structures with even number of carbon atoms, for example, consider the structure:
Here, the relative position of the hydrogen atom is indicated as follows:
For structures with an odd number of carbon atoms, for example, consider the structure:
Here, the relative position of the hydrogen atom is indicated as follows:
Thus structures with even a number of carbon atoms as in
Want to see more full solutions like this?
Chapter 2 Solutions
CHEMICAL PRINCIPLES (LL) W/ACCESS
- a. What is the eluent used in the column chromatography here (a “silica plug filtration” is essentially a very short column)? b. The spectroscopy of compound 5b is described in the second half of this excerpt, including 1H-NMR and 13C-NMR (which you will learn about in CHEM 2412L), MS (which you will learn about later in CHEM 2411L) and IR. One of the IR signals is at 3530 cm-1. What functional group does this indicate might be present in compound 5b?arrow_forwardSteps and explanations. Also provide, if possible, ways to adress this kind of problems in general.arrow_forwarda. The first three lines of this procedure describe the reaction used to make compound 5b. In the fourth line, hexane and sodium bicarbonate are added. What organic lab technique is being used here? b. What is the purpose of the Na2SO4? c. What equipment would you use to “concentrate [a solution] under reduced pressure”?arrow_forward
- When N,N-dimethylaniline is treated with bromine both the ortho and para products are observed. However when treated with a mixture of nitric acid and sulfuric acid only the meta product is observed. Explain these results and support your answer with the appropriate drawings *Hint amines are bases* N HNO3 H2SO4 N NO2 N Br2 N Br + N 8-8-8 FeBr3 Brarrow_forwardDraw a mechanism that explains the formation of compound OMe SO3H 1. Fuming H2SO4arrow_forwardConsider the following two acid-base reactions: OH OHI Based on what you know about the compounds and their acidity, which direction would you expect both of these reactions to proceed? Show your reasoning. A pKa table has been provided in case you need it. Functional group Example pka CHA -50 Alkane -35 Amine : NH3 Alkyne RH 25 Water HO-H 169 16 10 Protonated amines NH 10 5 Carboxylic acids OH Hydrochloric acid HCI A chemist intends to run the following reaction on the three substrates shown below: H₂O R-CI product room temp. Cl Cl (1) (2) (3) They find one will react quickly, one slowly, and one will not react at all. Which is which, and why? HINT: What is the reaction they're trying to do? Does that mechanism tell you anything about why something would be favored?arrow_forward
- NH3 decomposes through an equilibrium reaction between NH3, H2, and N2. Only one of the options is correct:(A). The mechanism of the NH3 decomposition reaction must necessarily involve the collision of two NH3 molecules to induce a rearrangement of the atoms in this molecule.(B). The molecular weight of the NH3 decomposition reaction is 2 since two NH3 molecules must collide.(C). The rate of the NH3 decomposition reaction must be greater than that of NH3 synthesis, since the former requires two molecules to collide and the latter, four.(D). The NH3 decomposition reaction cannot occur in a single step.arrow_forwardGiven the equilibrium A2 + B2 ⇌ 2 AB where k1 is the rate coefficient of the forward reaction and k-1 is the rate coefficient of the reverse reaction, with the forward reaction being first-order in A2 and B2, and the reverse reaction being second-order in AB. Equilibrium will be reached later if the relative values of the constants are:(A) k1 high and k-1 high(B) k1 high and k-1 low(C) k1 low and k-1 high(D) k1 low and k-1 lowarrow_forwardA 2-step reaction has the following mechanism: | 1. (fast) R2 R+R 2. (slow) R+Q K₂ P k_1 What series does it have? (A). v= - = (k + k1 − k-1)[R2][Q] (B). v=-k₁[R₂] + k₁[R]² - k₂[R][Q] (C). v=k₂[R]²[Q]² (D). v = k[R₂]1/2[Q]arrow_forward
- Steps and explanations. Also provide, if possible, ways to adress this kind of problems in general.arrow_forwardSteps and explanations. Also provide, if possible, ways to adress this kind of problems in general.arrow_forwardSteps and explanations. Also provide, if possible, ways to adress this kind of problems in general.arrow_forward
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningChemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning

