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Concept explainers
(a)
Interpretation:
The name of the following aldehyde is to be determined.
Concept Introduction:
While naming the
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Answer to Problem 16.32P
The name of the compound is 3,3-dimethylbutanal.
Explanation of Solution
The given molecular formula of the aldehyde is:
Here the numbering of the carbon chain will start from the right where -CHO group is present. It can be clearly seen that the longest carbon chain containing the aldehyde group consists of four carbon atoms and two methyl substituentsare attached to carbon number 3.
Therefore, the name of the compound becomes 3,3-dimethylbutanal.
(b)
Interpretation:
The name of the following aldehyde is to be determined.
Concept Introduction:
While naming the aldehydes as per the IUPAC nomenclature, the naming of the compounds is done by adding a suffix-al in the end of the name. Firstly, one will find the longest chain that contains the -CHO group and then change the -e ending of the parent alkane chain to -al suffix. Then, the numbering of the chain or the ring is done in such a way so as to put the -CHO group at carbon number 1 followed by omitting this number from the name. Thereafter, apply all other rules of nomenclature as usual.
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Answer to Problem 16.32P
The name of the compound is 4-ethylheaxanal.
Explanation of Solution
The given molecular formula of the aldehyde is:
Here the numbering of the carbon chain will start from the right where -CHO group is present. It can be clearly seen that the longest carbon chain containing aldehydic group consists of six carbon atoms and an ethyl substituent is attached to carbon number4.
Therefore, the name of the compound becomes 4-ethylhexanal.
(c)
Interpretation:
The name of the following aldehyde is to be determined.
Concept Introduction:
While naming the aldehydes as per the IUPAC nomenclature, the naming of the compounds is done by adding a suffix-al in the end of the name. Firstly, one will find the longest chain that contains the -CHO group and then change the -e ending of the parent alkane chain to -al suffix. Then, the numbering of the chain or the ring is done in such a way so as to put the -CHO group at carbon no. 1 followed by omitting this number from the name. Thereafter, apply all other rules of nomenclature as usual.
![Check Mark](/static/check-mark.png)
Answer to Problem 16.32P
The name of the compound is 3,4-dimethyloctanal.
Explanation of Solution
The given molecular formula of the aldehyde is:
Here, the numbering of the carbon chain will start from the right where -CHO group is present. It can be clearly seen that the longest carbon chain containing the aldehyde group consists of eight carbon atoms and a methyl substituent is attached to carbon number 3 as well as carbon number 4.
Therefore, the name of the compound becomes 3,4-dimethyloctanal.
(d)
Interpretation:
The name of the following aldehyde is to be determined.
Concept Introduction:
While naming the aldehydes as per the IUPAC nomenclature, the naming of the compounds is done by adding a suffix-al in the end of the name. Firstly, one will find the longest chain that contains the -CHO group and then change the -e ending of the parent alkane chain to -al suffix. Then, the numbering of the chain or the ring is done in such a way so as to put the -CHO group at carbon number 1 followed by omitting this number from the name. Thereafter, apply all other rules of nomenclature as usual.
![Check Mark](/static/check-mark.png)
Answer to Problem 16.32P
The name of the compound is 3-butylheptanal.
Explanation of Solution
The given molecular formula of the aldehyde can be written as follows:
Here, the numbering of the carbon chain will start from the right where -CHO group is present. It can be clearly seen that the longest carbon chain containing the aldehyde group consists of seven carbon atoms and abutyl substituent is attached to carbon number 3.
Therefore, the name of the compound becomes 3-butylheptanal.
(e)
Interpretation:
The name of the following aldehyde is to be determined.
Concept Introduction:
While naming the aldehydes as per the IUPAC nomenclature, the naming of the compounds is done by adding a suffix-al in the end of the name. Firstly, one will find the longest chain that contains the -CHO group and then change the -e ending of the parent alkane chain to -al suffix. Then, the numbering of the chain or the ring is done in such a way so as to put the -CHO group at carbon no. 1 followed by omitting this number from the name. Thereafter, apply all other rules of nomenclature as usual.
![Check Mark](/static/check-mark.png)
Answer to Problem 16.32P
The name of the compound is 3-ethylbenzaldehyde.
Explanation of Solution
The given molecular formula of the aldehyde is:
The name of the compound will be 3-ethylbenzaldehyde as the ethyl group is attached to the carbon number 3 of the parent molecule which is benzaldehyde. The benzene ring when attached to -CHO group is known as benzaldehyde.
The naming of the molecule will start from the carbon to which aldehydic group is attached.
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Chapter 16 Solutions
EBK GENERAL, ORGANIC, & BIOLOGICAL CHEM
- X Draw the major products of the elimination reaction below. If elimination would not occur at a significant rate, check the box under the drawing area instead. ది www. Cl + OH Elimination will not occur at a significant rate. Click and drag to start drawing a structure.arrow_forwardNonearrow_forward1A H 2A Li Be Use the References to access important values if needed for this question. 8A 3A 4A 5A 6A 7A He B C N O F Ne Na Mg 3B 4B 5B 6B 7B 8B-1B 2B Al Si P 1B 2B Al Si P S Cl Ar K Ca Sc Ti V Cr Mn Fe Co Ni Cu Zn Ga Ge As Se Br Kr Rb Sr Y Zr Nb Mo Tc Ru Rh Pd Ag Cd In Sn Sb Te I Xe * Cs Ba La Hf Ta W Re Os Ir Pt Au Hg Tl Pb Bi Po At Rn Fr Ra Ac Rf Ha ****** Ce Pr Nd Pm Sm Eu Gd Tb Dy Ho Er Tm Yb Lu Th Pa U Np Pu Am Cm Bk Cf Es Fm Md No Lr Analyze the following reaction by looking at the electron configurations given below each box. Put a number and a symbol in each box to show the number and kind of the corresponding atom or ion. Use the smallest integers possible. cation anion + + Shell 1: 2 Shell 2: 8 Shell 3: 1 Shell 1 : 2 Shell 2 : 6 Shell 1 : 2 Shell 2: 8 Shell 1: 2 Shell 2: 8arrow_forward
- Nonearrow_forwardIV. Show the detailed synthesis strategy for the following compounds. a. CH3CH2CH2CH2Br CH3CH2CCH2CH2CH3arrow_forwardDo the electrons on the OH participate in resonance with the ring through a p orbital? How many pi electrons are in the ring, 4 (from the two double bonds) or 6 (including the electrons on the O)?arrow_forward
- Predict and draw the product of the following organic reaction:arrow_forwardNonearrow_forwardRedraw the molecule below as a skeletal ("line") structure. Be sure to use wedge and dash bonds if necessary to accurately represent the direction of the bonds to ring substituents. Cl. Br Click and drag to start drawing a structure. : ☐ ☑ Parrow_forward
- K m Choose the best reagents to complete the following reaction. L ZI 0 Problem 4 of 11 A 1. NaOH 2. CH3CH2CH2NH2 1. HCI B OH 2. CH3CH2CH2NH2 DII F1 F2 F3 F4 F5 A F6 C CH3CH2CH2NH2 1. SOCl2 D 2. CH3CH2CH2NH2 1. CH3CH2CH2NH2 E 2. SOCl2 Done PrtScn Home End FA FQ 510 * PgUp M Submit PgDn F11arrow_forwardNonearrow_forwardPlease provide a mechanism of synthesis 1,4-diaminobenzene, start from a benzene ring.arrow_forward
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