(a)
Interpretation: The name of the following aromatic compound should be determined:
Concept Introduction: The ring structures of the compound having uncommon stability due to delocalized pi electron density shared in between all the carbon atoms of the ring is said to be an aromatic compound.
In order to give the name to the multiple substituted
- For single substituted aromatic compound (when the substituent contains six or fewer carbons), the name of the substituted group is written first followed by the name of the aromatic compound.
- For single substituted aromatic compound (when the substituent contains more than six carbons), the name of the aromatic compound is written first followed by the name of the substituted group.
- For single substituted aromatic compound, the numbering on the ring is done in such a way that the multiple substituents get the lowest number.
(b)
Interpretation: The name of the following aromatic compound should be determined:
Concept Introduction: The ring structures of the compound having uncommon stability due to delocalized pi electron density shared in between all the carbon atoms of the ring is said to be an aromatic compound.
In order to give the name to the multiple substituted aromatic compounds, the following steps are followed:
- For single substituted aromatic compound (when the substituent contains six or fewer carbons), the name of the substituted group is written first followed by the name of the aromatic compound.
- For single substituted aromatic compound (when the substituent contains more than six carbons), the name of the aromatic compound is written first followed by the name of the substituted group.
- For single substituted aromatic compound, the numbering on the ring is done in such a way that the multiple substituents get the lowest number.
(c)
Interpretation: The name of the following aromatic compound should be determined:
Concept Introduction: The ring structures of the compound having uncommon stability due to delocalized pi electron density shared in between all the carbon atoms of the ring is said to be an aromatic compound.
In order to give the name to the multiple substituted aromatic compounds, the following steps are followed:
- For single substituted aromatic compound (when the substituent contains six or fewer carbons), the name of the substituted group is written first followed by the name of the aromatic compound.
- For single substituted aromatic compound (when the substituent contains more than six carbons), the name of the aromatic compound is written first followed by the name of the substituted group.
- For single substituted aromatic compound, the numbering on the ring is done in such a way that the multiple substituents get the lowest number.
Want to see the full answer?
Check out a sample textbook solutionChapter 17 Solutions
Basic Chemistry
- Rank the following substances in order of increasing acidity: Which, if any, of the four compounds is a strong enough acid to react almost completely OH CHyCH3 CHyČCH,ČCH, CH,COH Acetone Pentane-2,4-dione Phenol Acetic acid with NaOH? (pK, 19.3) (pK, = 9) (pK, = 9.9) (pK,4.76) (The pK, of H20 is 15.74.)arrow_forwardSimple alcohols (just containing C's, H's and an OH, where the H on the O is the acidic H) have a pKa similar to water (15.7) hydronium ion (-2)arrow_forward(12.9) Which of the following has the highest boiling point? O Both H₂S and H₂O have the same boiling point that is higher than the boiling point of H₂Se. O H₂Se O H₂O O H₂Sarrow_forward
- 12:46 16.48 Give the IUPAC and common names, if any, for each of the following compounds: (16.1, 16.4) CH3 a. CH3-CH-CH2-CH2-c-OH hey C- HO- b. Cl d. CH3-CH2–CH2-C-0–CH3 CH3 C-0-CH,-CH3 e. CH3-CH – CH2 CH3 OH f. CH3 CH- CH2 -СН-С-ОНarrow_forwardChem help! 7.6arrow_forward7. What is the ordered pair corresponding to the point marked "A" in this А. (4, 14.0) В. (4, 10.4) С. (4, 5.1) D. (4, 4.1) graph? 10 10 10° 1 3 4 6 9. 10 8. How much kinetic energy does an electron (m = 9.1x10 kg) have if it is A. 1.0x1014 B. 1.4x10" J C. 2.7x102 J D. 6.8x10* J J traveling at one-half the speed of light?arrow_forward
- Give only typing answer with explanation and conclusion Which of the following statements is/are incorrect? (6,25 p) I- In order for an organic compound to be a dyestuff, it must be chromor and auxochrochrome. II- Hydroxyl or amino groups can be given as examples of chromophore groups III- Decrease of chromophore groups in a molecule causes color deepening. A. b) II, III B. a) I only C. d) II only D. c) III onlyarrow_forwardwhat starting materials and reagents could form the indicated product ? Fill in the reaction, acco unt for H indicated as being from the reaction 1.2.3.4.5arrow_forwardSolve the following three problems. 11.4, 11.5,11.6arrow_forward
- Help me with all please !!! (1 to 5)arrow_forward5.45 A, B, Carrow_forward6. (4 pts) Which one of these is most likely to smell bad? ) Amines with more than six carb b) aqueous HCI c) aqued a) water a) butyl amine c) N-butylbutanamide b) butyl butanoate d) sodium butanoate Saponification" may be defined as: pasic hydrolysis of an ester b) basic hydrolysis of an amide c) reduction of an ester d) reduction of an amide Condensation" polymers are called that because: a) they are smaller than other polymers d) they are only made in labs In carhons in the starting materials.arrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY