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Concept explainers
(a)
Interpretation:
The eight alcohols have to be written with the molecular formula of
Concept introduction:
Isomer: A molecule having same molecular formula with different chemical formula is called isomer.
Alcohol:
The compound contains hydroxyl
Example is given below,
(b)
Interpretation:
Eight aldehydeswith the molecular formula of
Concept introduction:
Isomer: A molecule having same molecular formula with different chemical formula is called isomer.
Functional group: They are certain substitutes in the organic molecules which are determine the characteristic reactions taking place in it.
Carbonyl group:
A carbon atom is double-bonded to an oxygen atom
If the carbonyl carbon is attached with two alkyl or aryl group is called as
(c)
Interpretation:
Six ketones have to be written with the molecular formula of
Concept introduction:
Isomer: A molecule having same molecular formula with different chemical formula is called isomer.
Functional group: They are certain substitutes in the organic molecules which are determine the characteristic reactions taking place in it.
Carbonyl group:
A carbon atom is double-bonded to an oxygen atom
If the carbonyl carbon is attached with two alkyl or aryl group is called as ketone, if the carbonyl carbon is attached with one hydrogen atom and one alkyl or aryl group is called as aldehyde.
(d)
Interpretation:
Eight
Concept introduction:
Isomer: A molecule having same molecular formula with different chemical formula is called isomer.
Functional group: They are certain substitutes in the organic molecules which are determine the characteristic reactions taking place in it.
Carboxylic acid:
A carbon atom is double-bonded to an oxygen atom
If the carbonyl carbon is attached with hydroxyl group is called as carboxylic acid.
(e)
Interpretation:
Nine carboxylic estershave to be written with the molecular formula of
Concept introduction:
Isomer: A molecule having same molecular formula with different chemical formula is called isomer.
Functional group: They are certain substitutes in the organic molecules which are determine the characteristic reactions taking place in it.
Carboxylic ester:
A carbon atom is double-bonded to an oxygen atom
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Chapter 1 Solutions
Organic Chemistry, Loose-leaf Version
- 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
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningOrganic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning
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