
Concept explainers
Interpretation:
The groups that has to be considered as substituents and the name for them has to be given.
Concept Introduction:
All the molecules have their unique names. These names must be known in order to communicate. But remembering all the chemical names is impossible as there are many numbers of molecules. To avoid this, the
Stereoisomerism | Substituents | Parent | Unsaturation | Functional Group |
Stereoisomerism indicate if the considered molecule has any stereocenters are present (R,S) and if double bond is present are cis/trans.
The groups that are connected to the main carbon chain is known as substituents. The substituents are identified after the carbon chain is identified and the functional group present in the given compound also identified. The substituents are named by adding “yl” to the end of the name which indicate that it is a substituent is an alkyl. The
The longest carbon chain is known as the parent. Parent carbon chain is the lengthiest carbon chain in the molecule that must include the functional group that is present in the compound. The longest carbon chain is identified and the parent name is given by the number of carbon atoms that is present in it. It must be remembered that even though functional group is not present in parent carbon chain, the double bond, triple bond if present has to be included.
Number of carbon atoms in chain | Parent |
1 | Meth |
2 | Eth |
3 | Prop |
4 | But |
5 | Pent |
6 | Hex |
Unsaturation indicates that if any triple or double bonds are present in the molecule. If a compound contains a double bond it is named as “-en-” and if a triple bond is present “-yn-” is used. If a compound contains two double bonds, then it is named as “-dien-”. If three double bonds are present in the given compound, then it is named as “-trien-”. This same rule applies for the compound that contains multiple triple bonds also.
Functional group is the one after which the considered compound is being named.
Functional Group | Class of compound | Suffix |
![]() | Ester | -oate |
![]() | Ketone | -one |
![]() | Aldehyde | -al |
![]() | -oic acid | |
![]() | Alcohol | -ol |
![]() | -amine |

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Chapter 5 Solutions
Organic Chemistry As a Second Language: First Semester Topics
- 151.2 254.8 85.9 199.6 241.4 87.6 242.5 186.4 155.8 257.1 242.9 253.3 256.0 216.6 108.7 239.0 149.7 236.4 152.1 222.7 148.7 278.2 268.7 234.4 262.7 283.2 143.6 QUESTION: Using this group of data on salt reduced tomato sauce concentration readings answer the following questions: 1. 95% Cl Confidence Interval (mmol/L) 2. [Na+] (mg/100 mL) 3. 95% Na+ Confidence Interval (mg/100 mL)arrow_forwardResults Search Results Best Free Coursehero Unloc xb Success Confirmation of Q x O Google Pas alekscgi/x/lsl.exe/1o_u-IgNslkr 7j8P3jH-IQs_pBanHhvlTCeeBZbufu BYTI0Hz7m7D3ZcHYUt80XL-5alyVpwDXM TEZayFYCavJ17dZtpxbFD0Qggd1J O States of Matter Using a phase diagram to find a phase transition temperature or pressure Gabr 3/5 he pressure above a pure sample of solid Substance X at 101. °C is lowered. At what pressure will the sample sublime? Use the phase diagram of X below to nd your answer. pressure (atm) 24- 12 solid liquid gas 200 400 temperature (K) 600 ote: your answer must be within 0.15 atm of the exact answer to be graded correct. atm Thanation Check © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center I Q Search L³ ملةarrow_forward301.7 348.9 193.7 308.6 339.5 160.6 337.7 464.7 223.5 370.5 326.6 327.5 336.1 317.9 203.8 329.8 221.9 331.7 211.7 309.6 223.4 353.7 334.6 305.6 340.0 304.3 244.7 QUESTION: Using this group of data on regular tomato sauce concentration readings answer the following questions: 1. 95% Cl Confidence Interval (mmol/L) 2. [Na+] (mg/100 mL) 3. 95% Na+ Confidence Interval (mg/100 mL)arrow_forward
- Search Results Search Results Best Free Coursehero Unlo x b Success Confirmation of Q aleks.com/alekscgi/x/sl.exe/10_u-lgNslkr7j8P3jH-IQs_pBan HhvlTCeeBZbufu BYTIOHz7m7D3ZcHYUt80XL-5alyVpwDXM TEZayFYCav States of Matter Using a phase diagram to find a phase transition temperature or pressure Use the phase diagram of Substance X below to find the temperature at which X turns to a gas, if the pressure above the solid is 3.7 atm. pressure (atm) 0. 32- 16 solid liquid gas 200 temperature (K) Note: your answer must be within 20 °C of the exact answer to be graded correct. Дос Xarrow_forwardConsider the reaction below to answer the following questions: Acetoacetic ester can be prepared by the Claisen self-condensation reaction of ethyl acetate. 1. NaOEt, EtOH H&C OCH CH3 2 H30 H3C CH2 OCH2CH3 A. Write the complete stepwise mechanism for this reaction. Show all electron flow with arrows and draw all intermediate structures. B. Ethyl acetate can be prepared from ethanol as the only organic starting material. Show all reagents and structures for all intermediates in this preparation. C. Give the structures of the ester precursors for the following Claisen condensation product and formulate the reaction. OEtarrow_forwardUse the phase diagram of Substance X below to find the temperature at which X turns to a gas, if the pressure above the solid is 3.7 atm. pressure (atm) 32 16 solid liquid gas 0 0 200 temperature (K) Note: your answer must be within 20 °C of the exact answer to be graded correct. Шос ☑ كarrow_forward
- Starting from bromoethane, how could you prepare the following compounds: a. Ethanol. b. Acetaldehyde f. Acetone. e. 2-Propanol i. Acetoacetic ester. d. 2-Bromoacetic acid. c. Acetic acid g. Acetamide. j. Ethylmalonate k. Gama ketoacid. h. Ethyl magnesium bromide.arrow_forward- The pressure above a pure sample of solid Substance X at 60. °C is raised. At what pressure will the sample melt? Use the phase diagram of X below to find your answer. pressure (atm) 02 0.4 solid Hliquid gas 0 0 200 400 600 temperature (K) Note: your answer must be within 0.025 atm of the exact answer to be graded correct. ☐ atmarrow_forward15. What is the order of decreasing reactivity towards nucleophilic acyl substitution for the carboxylic acid derivatives? (most reactive first) 0 O H3C COC CH3 H₂C C N(CH3)2 H3C C OCH3 A. a. I, 11, 111, b. I, III, IV, II C. II, IV, III, I ° (CH3)2CH C OCH3 IV d. II, I, III, IV B. R COCR 0 0 0 13= RC NH2 RC OR RC CI === IV a. I, III, II, IV b. II, III, I, IV C. III, II, I, IV d. IV, I, III, IIarrow_forward
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