General, Organic, and Biological Chemistry - 4th edition
4th Edition
ISBN: 9781259883989
Author: by Janice Smith
Publisher: McGraw-Hill Education
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Chapter 13, Problem 28P
Give the IUPAC name for each molecule depicted in the ball-and-stick models.
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Give the IUPAC name for each molecule depicted in the ball-and-stick models.
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1st isomer: has quarternary, secondary, and primary carbons
2nd isomer: has secondary and primary carbons
Chapter 13 Solutions
General, Organic, and Biological Chemistry - 4th edition
Ch. 13.1 - Convert each condensed structure to a complete...Ch. 13.1 - Prob. 13.1PCh. 13.1 - Complete the structure of zingiberene, a component...Ch. 13.2 - Prob. 13.2PPCh. 13.2 - Prob. 13.3PCh. 13.2 - Prob. 13.3PPCh. 13.2 - Prob. 13.4PPCh. 13.3 - Prob. 13.5PPCh. 13.3 - Prob. 13.4PCh. 13.3 - Prob. 13.6PP
Ch. 13.3 - Prob. 13.5PCh. 13.3 - Prob. 13.6PCh. 13.3 - Prob. 13.7PCh. 13.3 - Prob. 13.8PCh. 13.6 - Prob. 13.7PPCh. 13.6 - Prob. 13.9PCh. 13.6 - What products is formed in each of the following...Ch. 13.6 - Prob. 13.9PPCh. 13.6 - What product is formed when l-pentene (CH3CH2CH2CH...Ch. 13.7 - Prob. 13.11PCh. 13.8 - Prob. 13.10PPCh. 13.8 - Prob. 13.12PCh. 13.8 - Prob. 13.13PCh. 13.10 - Prob. 13.11PPCh. 13.10 - Prob. 13.14PCh. 13.11 - Prob. 13.15PCh. 13.12 - Prob. 13.16PCh. 13.13 - Prob. 13.17PCh. 13.13 - Prob. 13.18PCh. 13 - Anethole, the major constituent of anise oil, is...Ch. 13 - Prob. 20PCh. 13 - What is the molecular formula for a hydrocarbon...Ch. 13 - Prob. 22PCh. 13 - Prob. 23PCh. 13 - Prob. 24PCh. 13 - Prob. 25PCh. 13 - Prob. 26PCh. 13 - Give the IUPAC name for each molecule depicted in...Ch. 13 - Give the IUPAC name for each molecule depicted in...Ch. 13 - Give the IUPAC name for each compound. a....Ch. 13 - Give the IUPAC name for each compound. d....Ch. 13 - Give the IUPAC name for each alkene.Ch. 13 - Give the I UP AC name for each alkene.Ch. 13 - Give the IUPAC name for each cyclic compound.Ch. 13 - Give the IUPAC name for each cyclic compound.Ch. 13 - Give the structure corresponding to each IUPAC...Ch. 13 - Prob. 36PCh. 13 - Each of the following IUPAC names is incorrect....Ch. 13 - Each of the following IUPAC names is incorrect....Ch. 13 - Prob. 39PCh. 13 - Prob. 40PCh. 13 - Prob. 41PCh. 13 - Prob. 42PCh. 13 - Prob. 43PCh. 13 - Label the carbon-carbon double bond as cis or...Ch. 13 - Prob. 45PCh. 13 - Prob. 46PCh. 13 - Prob. 47PCh. 13 - Prob. 48PCh. 13 - Prob. 49PCh. 13 - Prob. 50PCh. 13 - Prob. 51PCh. 13 - Prob. 52PCh. 13 - Prob. 53PCh. 13 - Prob. 54PCh. 13 - What alkyd halide is formed when each alkene is...Ch. 13 - Prob. 56PCh. 13 - Prob. 57PCh. 13 - Prob. 58PCh. 13 - What alkene is needed as a starting material to...Ch. 13 - Prob. 60PCh. 13 - Prob. 61PCh. 13 - Prob. 62PCh. 13 - Prob. 63PCh. 13 - Prob. 64PCh. 13 - Prob. 65PCh. 13 - Prob. 66PCh. 13 - Prob. 67PCh. 13 - Prob. 68PCh. 13 - Prob. 69PCh. 13 - Prob. 70PCh. 13 - Prob. 71PCh. 13 - Prob. 72PCh. 13 - Prob. 73PCh. 13 - Are o-bromochlorobenzene and m-bromochlorobenzene...Ch. 13 - Give the structure corresponding to each IUPAC...Ch. 13 - Give the structure corresponding to each IUPAC...Ch. 13 - Prob. 77PCh. 13 - Prob. 78PCh. 13 - Prob. 79PCh. 13 - Prob. 80PCh. 13 - Prob. 81PCh. 13 - Prob. 82PCh. 13 - Prob. 83PCh. 13 - Prob. 84PCh. 13 - Prob. 85PCh. 13 - Eleostearic acid is an unsaturated fatty acid...Ch. 13 - Prob. 87PCh. 13 - Prob. 88PCh. 13 - Prob. 89PCh. 13 - Prob. 90PCh. 13 - Prob. 91PCh. 13 - Prob. 92PCh. 13 - Prob. 93PCh. 13 - Prob. 94PCh. 13 - Answer the following questions about compound A,...Ch. 13 - Prob. 96PCh. 13 - Answer the following questions about alkene C,...Ch. 13 - Prob. 98PCh. 13 - Prob. 99PCh. 13 - Prob. 100PCh. 13 - Prob. 101CPCh. 13 - Prob. 102CP
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- Give the IUPAC name.arrow_forwardComplete the IUPAC Name of the structure.arrow_forwardWhat is the IUPAC name for the compound shown? Step 1: Identify the number of carbons in the longest chain Step 2: Identify the base name of the molecule. Step 3: Number the longest chain. Step 4: Identify substituents. Step 5: Order the substituents. Step 6: Add the substituent locants or numbering. Step 7: Put it all together and give the IUPAC name. Step 7: Put it all together and give the IUPAC name. You have determined the name of the longest carbon chain and the locations and name of the substituents. Complete the name of the molecule by adding in the hyphens and commas. 3ethyl223trimethyl5propyldecane 3-ethyl,2,2,3trimethyl-5propyldecane IUPAC name: Incorrectarrow_forward
- What is the IUPAC name for the compound shown? Step 1: Identify the number of carbons in the longest chain Step 2: Identify the base name of the molecule. Step 3: Number the longest chain. Step 4: Identify substituents. Step 5: Order the substituents. Step 6: Add the substituent locants or numbering. Step 7: Put it all together and give the IUPAC name. Step 7: Put it all together and give the IUPAC name. You have determined the name of the longest carbon chain and the locations and name of the substituents. Complete the name of the molecule by adding in the hyphens and commas. 3ethyl223trimethyl5propyldecane JUPAC name:arrow_forwardWhat is the IUPAC name for this compound. Include 'cis' and trans'.arrow_forwardWhat is the IUPAC name for the compound shown? Step 1: Identify the number of carbons in the longest chain Step 2: Identify the base name of the molecule. Step 3: Number the longest chain. Step 4: Identify substituents. Step 5: Order the substituents. Step 6: Add the substituent locants or numbering. Step 7: Put it all together and give the IUPAC name. Step 5: Order the substituents. Since there are multiple substituents present, we must next consider the order the substituents in the name. The substituent order should be methyl, ethyl, followed by propyl ethyl, propyl, followed by trimethyl trimethyl, ethyl followed by propyl O ethyl, trimethyl, followed by propylarrow_forward
- What is the IUPAC name for the compound shown? Step 1: Identify the number of carbons in the longest chain Step 2: Identify the base name of the molecule. Step 3: Number the longest chain. Step 4: Identify substituents. Step 5: Order the substituents. Step 6: Add the substituent locants or numbering. Step 7: Put it all together and give the IUPAC name. Step 3: Number the longest chain of carbon atoms so that the substituents have the lowest possible numbers. Carbon atoms that are not in the longest chain should not be numbered. Answer Bank 10 5 3 8 2.arrow_forwardWhat is the IUPAC name for the compound shown? Step 1: Identify the number of carbons in the longest chain Step 2: Identify the base name of the molecule. Step 3: Number the longest chain. Step 4: Identify substituents. Step 5: Order the substituents. Step 6: Add the substituent locants or numbering. Step 7: Put it all together and give the IUPAC name. Step 6: Add the substituent locants or numbering. Now that you have identified the order of the substituents, you need to provide the locant, which indicates the number carbon on the main chain where each substituent is placed. Carbon 5 has only one substituent, so the name is represented by 5-propyl. Both carbons 2 and 3 have two substituents. What would be the correct naming for those carbons? The substituents should be named: 2,2-dimethyl and 3-methyl-3-ethyl 2,3-trimethyl and 3-ethyl 2,2,3-trimethyl and 3-ethyl 2-dimethyl and 3-methylethylarrow_forwardGive the common name for NN OH T CH3-CH₂-C-N-CH₂-CH3 Spell out the common name of the compound. Give the IUPAC name for 0 CH₂ || CH₂-C-N-CH₂-CH₂-CH₂, Spell out the IUPAC name of the compound. diethylamine Draw all missing reactants and/or products in the appropriate boxes by placing atoms on the canvas and connecting them with bonds. Add charges where needed. HE CONT HOarrow_forward
- Draw four constitutional isomers having molecular formula C 6H 12 that contain a four-membered ring. Give the IUPAC name for each isomer.arrow_forwarddraw the structure of two costitution isomers with the molecular formula of C4H10. Give the IUPAC name of each isomerarrow_forwardGive systematic (IUPAC) name for each compound. H₂C-Cl IUPAC name: CH3 HỌC–CH–CH,-CH-CH,CH, B,C-CH-CH Cl IUPAC name: CHIC IUPAC name:arrow_forward
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