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Concept explainers
Interpretation:
IHD for the compound having the molecular formula
Concept introduction:
In order to determine the IHD of a given molecular formula, first, draw any saturated molecule that has the same number of each non-hydrogen atom as in the given formula. The saturated molecule must not contain double bonds, triple bonds, or rings. Each atom should have its ‘normal’ number of bonds and lone pairs to avoid formal charges. Thus, each carbon should have four bonds, each hydrogen should have one bond, each oxygen should have two bonds and two lone pairs, each halogen must have one bond and three lone pairs of electrons while each nitrogen should have three bonds and one lone pair. The next step is to determine how many more hydrogen atoms are in this saturated molecule compared to the formula that is given. In the last step, the IHD is calculated by dividing that number of additional hydrogen atoms by 2.
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Chapter 4 Solutions
EBK ORGANIC CHEMISTRY: PRINCIPLES AND M
- 16. The proton NMR spectral information shown in this problem is for a compound with formula CioH,N. Expansions are shown for the region from 8.7 to 7.0 ppm. The normal carbon-13 spec- tral results, including DEPT-135 and DEPT-90 results, are tabulated: 7 J Normal Carbon DEPT-135 DEPT-90 19 ppm Positive No peak 122 Positive Positive cus и 124 Positive Positive 126 Positive Positive 128 No peak No peak 4° 129 Positive Positive 130 Positive Positive (144 No peak No peak 148 No peak No peak 150 Positive Positive してしarrow_forward3. Propose a synthesis for the following transformation. Do not draw an arrow-pushing mechanism below, but make sure to draw the product of each proposed step (3 points). + En CN CNarrow_forwardShow work..don't give Ai generated solution...arrow_forward
- Label the spectrum with spectroscopyarrow_forwardQ1: Draw the most stable and the least stable Newman projections about the C2-C3 bond for each of the following isomers (A-C). Are the barriers to rotation identical for enantiomers A and B? How about the diastereomers (A versus C or B versus C)? enantiomers H Br H Br (S) CH3 H3C (S) (R) CH3 H3C H Br A Br H C H Br H3C (R) B (R)CH3 H Br H Br H3C (R) (S) CH3 Br H D identicalarrow_forwardLabel the spectrumarrow_forward
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning
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