
Concept explainers
Interpretation:
The structure of the compound of molecular formula
Concept introduction:
Absorption of IR radiation causes excitations of vibrational motion of the atoms in a molecule. The vibrational motion can be of different types. In stretching vibrations, the bond length changes periodically. In bending vibrations, the bond angle or dihedral angle changes periodically. This may be an in-plane vibration or out of plane vibration.
The changes in the vibrational motion of the atoms in a molecule are quantized, i.e., the energy of vibrational motion can only have certain discrete values. In general, the frequency of the quantum of radiation absorbed and the frequency of vibration are the same.
The energy needed to excite molecular vibrations depends on the bond strength as a bond can be considered to behave like a spring. In turn, this also means it depends on the mass of the atoms that form the bond. In effect, this means the absorption peaks in the IR spectrum are characteristic of the bond between a particular pair of atoms. They are characteristic of the
An IR spectrum records percent transmittance as a function of the wavenumber
The index of hydrogen deficiency (IHD) of a molecule is calculated as the difference between the number of hydrogen atoms in the compound and the number of hydrogen atoms in the corresponding saturated compound divided by two. A double bond and a ring each contribute one to IHD. A triple bond contributes two to IHD.

Want to see the full answer?
Check out a sample textbook solution
Chapter 15 Solutions
Get Ready for Organic Chemistry
- A covalent bond is the result of the a) b) c) d) e) overlap of two half-filled s orbitals overlap of a half-filled s orbital and a half-filled p orbital overlap of two half-filled p orbitals along their axes parallel overlap of two half-filled parallel p orbitals all of the abovearrow_forwardCan the target compound at right be efficiently synthesized in good yield from the unsubstituted benzene at left? starting material target If so, draw a synthesis below. If no synthesis using reagents ALEKS recognizes is possible, check the box under the drawing area. Be sure you follow the standard ALEKS rules for submitting syntheses. + More... Note for advanced students: you may assume that you are using a large excess of benzene as your starting material. C T Add/Remove step X ноarrow_forwardWhich one of the following atoms should have the largest electron affinity? a) b) c) d) 으으 e) 1s² 2s² 2p6 3s¹ 1s² 2s² 2p5 1s² 2s² 2p 3s² 3p² 1s² 2s 2p 3s² 3p6 4s2 3ds 1s² 2s² 2p6arrow_forward
- All of the following are allowed energy levels except _. a) 3f b) 1s c) 3d d) 5p e) 6sarrow_forwardA student wants to make the following product in good yield from a single transformation step, starting from benzene. Add any organic reagents the student is missing on the left-hand side of the arrow, and any addition reagents that are necessary above or below the arrow. If this product can't be made in good yield with a single transformation step, check the box below the drawing area. Note for advanced students: you may assume that an excess of benzene is used as part of the reaction conditions. : ☐ + I X This product can't be made in a single transformation step.arrow_forwardPredict the major products of this organic reaction:arrow_forward
- Name the family to which each organic compound belongs. The first answer has been filled in for you. compound CH₂ || CH3-C-NH2 0 ။ CH3-C-CH₂ CH=O–CH=CH, CH₂ HO CH2-CH2-CH-CH3 family amine Darrow_forward1b. Br LOHarrow_forwardI would like my graphs checked please. Do they look right? Do I have iodine and persulfate on the right axis ?arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning

