(a)
Interpretation:
The CN stretching mode that absorbs the higher-frequency IR photons is to be indicated for given pair of compounds. The reason for it is to be explained.
Concept introduction:
We simplify the picture of molecular vibrations by considering the ball-and-spring model, which treats bonds as simple springs that connect atoms together. According to Hooke’s law, the spring vibrates at a particular frequency (

Answer to Problem 15.19P
The CN stretching mode that absorbs the higher-frequency IR photons due to strong and stiffer bond is indicated below,
Explanation of Solution
The given pair of compounds is,
The triple bonds tend to be stronger and stiffer than double bonds. A stronger and stiffer bond tends to lead to a higher vibrational frequency. In given pair of compounds, with the faster vibration, the
The CN stretching mode that absorbs the higher-frequency IR photons is shown below,
The CN stretching mode that absorbs the higher-frequency IR photons is indicated on the basis of the relationship between strength and stiffness of the bond and vibrational frequency.
(b)
Interpretation:
The CN stretching mode that absorbs the higher-frequency IR photons is to be indicated for given pair of compounds. The reason for it is to be explained.
Concept introduction:
We simplify the picture of molecular vibrations by considering the ball-and-spring model, which treats bonds as simple springs that connect atoms together. According to Hooke’s law, the spring vibrates at a particular frequency (

Answer to Problem 15.19P
The CN stretching mode that absorbs the higher-frequency IR photons due to strong and stiffer bond is indicated below,
Explanation of Solution
The given pair of compounds is,
The double bonds tend to be stronger and stiffer than single bonds. A stronger and stiffer bond tends to lead to a higher vibrational frequency. In given pair of compounds, with the faster vibration, the
The CN stretching mode that absorbs the higher-frequency IR photons is shown below,
The CN stretching mode that absorbs the higher-frequency IR photons is indicated on the basis of the relationship between strength and stiffness of the bond and vibrational frequency.
(c)
Interpretation:
The CN stretching mode that absorbs the higher-frequency IR photons is to be indicated for given pair of compounds. The reason for it is to be explained.
Concept introduction:
We simplify the picture of molecular vibrations by considering the ball-and-spring model, which treats bonds as simple springs that connect atoms together. According to Hooke’s law, the spring vibrates at a particular frequency (

Answer to Problem 15.19P
The CN stretching mode that absorbs the higher-frequency IR photons due to lower mass is indicated below,
Explanation of Solution
The given pair of compounds is,
In both compounds there is
But
The CN stretching mode that absorbs the higher-frequency IR photons is shown below,
The vibrational mode that absorbs at a higher frequency in the IR region is determined on the basis of the relationship between mass and vibrational frequency.
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Chapter 15 Solutions
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- Identify the unknown compound from its IR and proton NMR spectra. C4H6O: 'H NMR: 82.43 (1H, t, J = 2 Hz); 8 3.41 (3H, s); 8 4.10 (2H, d, J = 2 Hz) IR: 2125, 3300 cm¹ The C4H6O compound liberates a gas when treated with C2H5 MgBr. Draw the unknown compound. Select Draw с H Templates Morearrow_forwardPlease help with number 6 I got a negative number could that be right?arrow_forward1,4-Dimethyl-1,3-cyclohexadiene can undergo 1,2- or 1,4-addition with hydrogen halides. (a) 1,2-Addition i. Draw the carbocation intermediate(s) formed during the 1,2-addition of hydrobromic acid to 1,4-dimethyl-1,3-cyclohexadiene. ii. What is the major 1,2-addition product formed during the reaction in (i)? (b) 1,4-Addition i. Draw the carbocation intermediate(s) formed during the 1,4-addition of hydrobromic acid to 1,4-dimethyl-1,3-cyclohexadiene. ii. What is the major 1,4-addition product formed from the reaction in (i)? (c) What is the kinetic product from the reaction of one mole of hydrobromic acid with 1,4-dimethyl-1,3-cyclohexadiene? Explain your reasoning. (d) What is the thermodynamic product from the reaction of one mole of hydrobro-mic acid with 1,4-dimethyl-1,3-cyclohexadiene? Explain your reasoning. (e) What major product will result when 1,4-dimethyl-1,3-cyclohexadiene is treated with one mole of hydrobromic acid at - 78 deg * C ? Explain your reasoning.arrow_forward
- Give the product of the bimolecular elimination from each of the isomeric halogenated compounds. Reaction A Reaction B. КОВ CH₂ HotBu +B+ ко HOIBU +Br+ Templates More QQQ Select Cv Templates More Cras QQQ One of these compounds undergoes elimination 50x faster than the other. Which one and why? Reaction A because the conformation needed for elimination places the phenyl groups and to each other Reaction A because the conformation needed for elimination places the phenyl groups gauche to each other. ◇ Reaction B because the conformation needed for elimination places the phenyl groups gach to each other. Reaction B because the conformation needed for elimination places the phenyl groups anti to each other.arrow_forwardFive isomeric alkenes. A through each undergo catalytic hydrogenation to give 2-methylpentane The IR spectra of these five alkenes have the key absorptions (in cm Compound Compound A –912. (§), 994 (5), 1643 (%), 3077 (1) Compound B 833 (3), 1667 (W), 3050 (weak shoulder on C-Habsorption) Compound C Compound D) –714 (5), 1665 (w), 3010 (m) 885 (3), 1650 (m), 3086 (m) 967 (5), no aharption 1600 to 1700, 3040 (m) Compound K Match each compound to the data presented. Compound A Compound B Compound C Compound D Compoundarrow_forward7. The three sets of replicate results below were accumulated for the analysis of the same sample. Pool these data to obtain the most efficient estimate of the mean analyte content and the standard deviation. Lead content/ppm: Set 1 Set 2 Set 3 1. 9.76 9.87 9.85 2. 9.42 9.64 9.91 3. 9.53 9.71 9.42 9.81 9.49arrow_forward
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- A student proposes the transformation below in one step of an organic synthesis. There may be one or more reactants missing from the left-hand side, but there are no products missing from the right-hand side. There may also be catalysts, small inorganic reagents, and other important reaction conditions missing from the arrow. • Is the student's transformation possible? If not, check the box under the drawing area. • If the student's transformation is possible, then complete the reaction by adding any missing reactants to the left-hand side, and adding required catalysts, inorganic reagents, or other important reaction conditions above and below the arrow. • You do not need to balance the reaction, but be sure every important organic reactant or product is shown. + T G OH де OH This transformation can't be done in one step.arrow_forwardMacmillan Leaming Draw the major organic product of the reaction. 1. CH3CH2MgBr 2. H+ - G Select Draw Templates More H о QQarrow_forwardDraw the condensed structure of 3-hydroxy-2-butanone. Click anywhere to draw the first atom of your structure.arrow_forward
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