(a)
Interpretation:
Molecular formula of Ramelteon has to be written.
Concept Introduction:
Molecular formula shows that the actual number of atoms of each element that are present in a molecule of the compound.
(b)
Interpretation:
Number of
Concept Introduction:
The geometry of the central atom will be determined by counting the steric number followed by the hybridization state of that central atom and finally electronic arrangement of atoms in space.
The steric number is the combination of both number of
If the steric number is 4, the central atom is sp3 hybridized and the electronic arrangement of atoms in space (i.e. geometry) will be tetrahedral.
If the steric number is 3, the central atom is sp2 hybridized and the electronic arrangement of atoms in space (i.e. geometry) will be trigonal planar.
If the steric number is 2, the central atom is sp hybridized and the electronic arrangement of atoms in space (i.e. geometry) will be linear.
(c)
Interpretation:
Number of
Concept Introduction:
The geometry of the central atom will be determined by counting the steric number followed by the hybridization state of that central atom and finally electronic arrangement of atoms in space.
The steric number is the combination of both number of
If the steric number is 4, the central atom is
If the steric number is 3, the central atom is
If the steric number is 2, the central atom is
(d)
Interpretation:
Number of
Concept Introduction:
The geometry of the central atom will be determined by counting the steric number followed by the hybridization state of that central atom and finally electronic arrangement of atoms in space.
The steric number is the combination of both number of
If the steric number is 4, the central atom is sp3 hybridized and the electronic arrangement of atoms in space (i.e. geometry) will be tetrahedral.
If the steric number is 3, the central atom is sp2 hybridized and the electronic arrangement of atoms in space (i.e. geometry) will be trigonal planar.
If the steric number is 2, the central atom is
(e)
Interpretation:
The lone pair of electrons present in the given structure has to be identified.
Concept introduction:
The unshared electrons of an atom that does not involve in bonding are called lone pair.
Steps to determine the lone of pair of electrons,
- Appropriate valence electron has to be known.
- The actual number of valence electrons exhibited by the atom has to be known.
- Count the number of bonds and assign the number of lone pair.
A formal charge (FC) is the charge assigned to an atom in a molecule, irrespective of relative electronegativity by thinking that electrons in all
(f)
Interpretation:
The lone pair of electrons is delocalized or not has to be identified.
Concept introduction:
The unshared electrons of an atom that does not involve in bonding are called lone pair.
Steps to determine the lone of pair of electrons,
- Appropriate valence electron has to be known.
- The actual number of valence electrons exhibited by the atom has to be known.
- Count the number of bonds and assign the number of lone pair.
A formal charge (FC) is the charge assigned to an atom in a molecule, irrespective of relative electronegativity by thinking that electrons in all chemical bonds are shared equally among atoms. Electrons can be tracked by formal charge.
(g)
Interpretation:
Geometry of the atoms except hydrogen has to be identified.
Concept introduction:
The steric number is the combination of both number of
The geometry of the central atom will be determined by counting the steric number followed by the hybridization state of that central atom and finally electronic arrangement of atoms in space.
If the steric number is 4, the central atom is sp3 hybridized and the electronic arrangement of atoms in space (i.e. geometry) will be tetrahedral.
If the steric number is 3, the central atom is sp2 hybridized and the electronic arrangement of atoms in space (i.e. geometry) will be trigonal planar.
If the steric number is 2, the central atom is sp hybridized and the electronic arrangement of atoms in space (i.e. geometry) will be linear.
trigonal pyramidal(if one lone pair of electron is present).
bent geometry (if two lone pair of electrons are present).
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Chapter 2 Solutions
ORGANIC CHEMISTRY (LL) >CUSTOM PACKAGE<
- Explanation O Conjugated Pi Systems Deducing the reactants of a Diels-Alder reaction Can the molecule on the right-hand side of this organic reaction be made in good yield from no more than two reactants, in one step, by moderately heating the reactants? ? Δ If your answer is yes, then draw the reactant or reactants in the drawing area below. You can draw the reactants in any arrangement you like. • If your answer is no, check the box under the drawing area instead. Click and drag to start drawing a structure. Xarrow_forwardDiels Alder Cycloaddition: Focus on regiochemistry (problems E-F) –> match + of thedienophile and - of the diene while also considering stereochemistry (endo).arrow_forwardHELP! URGENT! PLEASE RESOND ASAP!arrow_forward
- Question 4 Determine the rate order and rate constant for sucrose hydrolysis. Time (hours) [C6H12O6] 0 0.501 0.500 0.451 1.00 0.404 1.50 0.363 3.00 0.267 First-order, k = 0.210 hour 1 First-order, k = 0.0912 hour 1 O Second-order, k = 0.590 M1 hour 1 O Zero-order, k = 0.0770 M/hour O Zero-order, k = 0.4896 M/hour O Second-order, k = 1.93 M-1-hour 1 10 ptsarrow_forwardDetermine the rate order and rate constant for sucrose hydrolysis. Time (hours) [C6H12O6] 0 0.501 0.500 0.451 1.00 0.404 1.50 0.363 3.00 0.267arrow_forwardDraw the products of the reaction shown below. Use wedge and dash bonds to indicate stereochemistry. Ignore inorganic byproducts. OSO4 (cat) (CH3)3COOH Select to Draw ઘarrow_forward
- Calculate the reaction rate for selenious acid, H2SeO3, if 0.1150 M I-1 decreases to 0.0770 M in 12.0 minutes. H2SeO3(aq) + 6I-1(aq) + 4H+1(aq) ⟶ Se(s) + 2I3-1(aq) + 3H2O(l)arrow_forwardProblem 5-31 Which of the following objects are chiral? (a) A basketball (d) A golf club (b) A fork (c) A wine glass (e) A spiral staircase (f) A snowflake Problem 5-32 Which of the following compounds are chiral? Draw them, and label the chirality centers. (a) 2,4-Dimethylheptane (b) 5-Ethyl-3,3-dimethylheptane (c) cis-1,4-Dichlorocyclohexane Problem 5-33 Draw chiral molecules that meet the following descriptions: (a) A chloroalkane, C5H11Cl (c) An alkene, C6H12 (b) An alcohol, C6H140 (d) An alkane, C8H18 Problem 5-36 Erythronolide B is the biological precursor of erythromycin, a broad-spectrum antibiotic. How H3C CH3 many chirality centers does erythronolide B have? OH Identify them. H3C -CH3 OH Erythronolide B H3C. H3C. OH OH CH3arrow_forwardPLEASE HELP! URGENT! PLEASE RESPOND!arrow_forward
- 2. Propose a mechanism for this reaction. ہلی سے ملی N H (excess)arrow_forwardSteps and explanationn please.arrow_forwardProblem 5-48 Assign R or S configurations to the chirality centers in ascorbic acid (vitamin C). OH H OH HO CH2OH Ascorbic acid O H Problem 5-49 Assign R or S stereochemistry to the chirality centers in the following Newman projections: H Cl H CH3 H3C. OH H3C (a) H H H3C (b) CH3 H Problem 5-52 Draw the meso form of each of the following molecules, and indicate the plane of symmetry in each: OH OH (a) CH3CHCH2CH2CHCH3 CH3 H3C. -OH (c) H3C CH3 (b) Problem 5-66 Assign R or S configurations to the chiral centers in cephalexin, trade-named Keflex, the most widely prescribed antibiotic in the United States. H2N H IHH S Cephalexin N. CH3 CO₂Harrow_forward
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