Chemistry: The Molecular Nature of Matter
7th Edition
ISBN: 9781118516461
Author: Neil D. Jespersen, Alison Hyslop
Publisher: WILEY
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Textbook Question
Chapter 22, Problem 4PE
Write the IUPAC names of the following compounds. In searching for the parent chain, be sure to look for the longest continuous chain of carbons even if the chain twists and goes around comers.
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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:
Analyze the structure of 4‑sec‑butyl-5-ethyl-3-methyloctane. Identify the number of ethyl and methyl groups in the compound. Note that these groups are not necessarily confined to those specifically mentioned in the name.
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
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Chapter 22 Solutions
Chemistry: The Molecular Nature of Matter
Ch. 22 - Prob. 1PECh. 22 - Prob. 2PECh. 22 - Prob. 3PECh. 22 - Practice Exercise 22.4
Write the IUPAC names of...Ch. 22 - Oxidation of an alcohol gave the following...Ch. 22 - Prob. 6PECh. 22 - Prob. 7PECh. 22 - Prob. 8PECh. 22 - Prob. 9PECh. 22 - Prob. 10PE
Ch. 22 - Complete the following equation by drawing...Ch. 22 - Prob. 12PECh. 22 - Prob. 13PECh. 22 - Prob. 14PECh. 22 - Prob. 15PECh. 22 - Label the hydrophobic and hydrophilic portions of...Ch. 22 - Draw a ribose ring and a deoxyribose ring. What is...Ch. 22 - Practice Exercise 22.18
Which base pairs match in...Ch. 22 - Prob. 1RQCh. 22 - Prob. 2RQCh. 22 - Prob. 3RQCh. 22 - Prob. 4RQCh. 22 - Prob. 5RQCh. 22 - Prob. 6RQCh. 22 - Prob. 7RQCh. 22 - Which of the following compounds has the higher...Ch. 22 - In general terms, why do functional groups impart...Ch. 22 - Prob. 10RQCh. 22 - What is the difference between geometric isomers...Ch. 22 - Prob. 12RQCh. 22 - No number is needed to identify the location of...Ch. 22 - Prob. 14RQCh. 22 - Prob. 15RQCh. 22 - Prob. 16RQCh. 22 - 22.17 In general terms, why doesn't benzene...Ch. 22 - Prob. 18RQCh. 22 - 22.19 Explain why is more soluble in water than ....Ch. 22 - Prob. 20RQCh. 22 - Prob. 21RQCh. 22 - Why do aldehydes and ketones have boiling points...Ch. 22 - Acetic acid boils at 118C, higher even than...Ch. 22 - Methyl ethanoate has many more atoms than its...Ch. 22 - Prob. 25RQCh. 22 - 22.26 Write condensed structures of the following...Ch. 22 - 3-Butanol is not a proper name, but a structure...Ch. 22 - Prob. 28RQCh. 22 - Prob. 29RQCh. 22 - Prob. 30RQCh. 22 - Prob. 31RQCh. 22 - Prob. 32RQCh. 22 - Amines, RNH2, do not have boiling points as high...Ch. 22 - A monofunctional organic nitrogen compound...Ch. 22 - Prob. 35RQCh. 22 - Prob. 36RQCh. 22 - Prob. 37RQCh. 22 - Write the products that can be expected to form in...Ch. 22 - Prob. 39RQCh. 22 - Prob. 40RQCh. 22 - 22.41 What do we mean by the term polymer...Ch. 22 - Prob. 42RQCh. 22 - Prob. 43RQCh. 22 - Prob. 44RQCh. 22 - Prob. 45RQCh. 22 - Prob. 46RQCh. 22 - Prob. 47RQCh. 22 - Prob. 48RQCh. 22 - Prob. 49RQCh. 22 - Prob. 50RQCh. 22 - Prob. 51RQCh. 22 - Prob. 52RQCh. 22 - Prob. 53RQCh. 22 - Prob. 54RQCh. 22 - Prob. 55RQCh. 22 - Prob. 56RQCh. 22 - Prob. 57RQCh. 22 - Prob. 58RQCh. 22 - What are the three fundamental needs for...Ch. 22 - Prob. 60RQCh. 22 - Prob. 61RQCh. 22 - Prob. 62RQCh. 22 - Name the compounds that form when sucrose is...Ch. 22 - Prob. 64RQCh. 22 - Prob. 65RQCh. 22 - Prob. 66RQCh. 22 - Prob. 67RQCh. 22 - 22.68 What function is served by glycogen in the...Ch. 22 - How are lipids defined?Ch. 22 - Why are lipids more soluble than carbohydrates in...Ch. 22 - 22.71 Cholesterol is not an ester, yet it is...Ch. 22 - A product such as corn oil is advertised as...Ch. 22 - Is it likely that the following compound could be...Ch. 22 - Describe the specific ways in which the monomers...Ch. 22 - What is the peptide bond? How is it similar to the...Ch. 22 - Prob. 76RQCh. 22 - Prob. 77RQCh. 22 - Why is a distinction made between the terms...Ch. 22 - Prob. 79RQCh. 22 - What kind of substance makes up most enzymes?Ch. 22 - Prob. 81RQCh. 22 - Prob. 82RQCh. 22 - Prob. 83RQCh. 22 - 22.84 How are the two DNA strands in a double...Ch. 22 - In what ways do DNA and RNA differ structurally.Ch. 22 - 22.86 Which base pairs with
Ch. 22 - The process of transcription begins with which...Ch. 22 - The process of translation begins with which...Ch. 22 - Prob. 89RQCh. 22 - 22.90 Write full (expanded) structures for each of...Ch. 22 - Prob. 91RQCh. 22 - Prob. 92RQCh. 22 - Prob. 93RQCh. 22 - Prob. 94RQCh. 22 - Prob. 95RQCh. 22 - Prob. 96RQCh. 22 - Prob. 97RQCh. 22 - Prob. 98RQCh. 22 - Prob. 99RQCh. 22 - Prob. 100RQCh. 22 - Prob. 101RQCh. 22 - 22.102 Write the structures of the cis and tram...Ch. 22 - 22.103 Write the structures of the products that...Ch. 22 - Prob. 104RQCh. 22 - 22.105 Repeat Problem 22.103 using...Ch. 22 - Repeat Problem 22.104 using cyclohexene. The...Ch. 22 - Prob. 107RQCh. 22 - Predict the products of the reaction of benzene...Ch. 22 - Prob. 109RQCh. 22 - Prob. 110RQCh. 22 - Prob. 111RQCh. 22 - Prob. 112RQCh. 22 - Prob. 113RQCh. 22 - Write the structure of the product of the...Ch. 22 - Prob. 115RQCh. 22 - Prob. 116RQCh. 22 - Prob. 117RQCh. 22 - Prob. 118RQCh. 22 - Prob. 119RQCh. 22 - Prob. 120RQCh. 22 - Prob. 121RQCh. 22 - Write the structures of the products that form in...Ch. 22 - Prob. 123RQCh. 22 - Prob. 124RQCh. 22 - Prob. 125RQCh. 22 - Prob. 126RQCh. 22 - Prob. 127RQCh. 22 - Prob. 128RQCh. 22 - 22.129 Write the structure of a triacylglycerol...Ch. 22 - 22.130 Write the structures of the products of the...Ch. 22 - Write the structure of the triacylglycerol that...Ch. 22 - *22.132 If the compound in Problem 22.130 is...Ch. 22 - *22.133 What parts of glyccrophospholipid...Ch. 22 - *22.134 In general terms, describe the structure...Ch. 22 - Prob. 135RQCh. 22 - What is the structure of the tripeptide that could...Ch. 22 - 22.137 What are the structures of the two...Ch. 22 - Prob. 138RQCh. 22 - Prob. 139RQCh. 22 - Prob. 140RQCh. 22 - Prob. 141RQCh. 22 - 22.142 Suggest a reason why trimethylamine, , has...Ch. 22 - Prob. 143RQCh. 22 - How many tripeptides can be made from three...Ch. 22 - Prob. 145RQCh. 22 - Prob. 146RQCh. 22 - Estimate the number of kilojoules of heat that...Ch. 22 - Prob. 148RQCh. 22 - Prob. 149RQCh. 22 - The compound that causes your eyes to water when...Ch. 22 - Prob. 151RQCh. 22 - Prob. 152RQCh. 22 - Use resonance structures to explain why urea,...Ch. 22 - Prob. 154RQCh. 22 - Prob. 155RQ
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- 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 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_forwardfind out correct and incorrect IUPAC name and give reason behind it!arrow_forwardUse the following description to determine the structure. Using your proposed structure determine the configuration (E or Z) of the alkene. An alkene that has a fluorine atom pointing back and a chlorine coming out on the leftmost carbon. The alkene also has a methyl group pointing back and an ethyl group coming out on the rightmost carbon. Use hydrogen fills the valence of carbon as needed.arrow_forward
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- I Review You may want to reference (Pages 399 - 404) Section 12.1 while completing this problem. Enter the IUPAC name for each of the following. Part A OH Spell out the full name of the compound. Submit Request Answer • Part B CH3 ÇH3 CH3-CH-CH2-CH–CH2-OH Spell out the full name of the compound. Submit Request Answer • Part C OH CH2-CH3 Spell out the full name of the compound. Submit Request Answerarrow_forwardGive IUPAC names for the following compounds. Part B CH,CH₂ CH₂SH CH₁ CH, Enter the correct IUPAC nomenclature.arrow_forwardPlease write the IUPAC name of the following compounds. Observe proper punctuations. Make sure that there are no spaces in between characters except those that have in their parent chain. Capitalize ONLY the first letter of the name. Also, don't use CIS/TRANS or E/Z in naming the compoundsarrow_forward
- Part L Give any common name for the following compound. Br CI If the compound has only the IUPAC name, enter no. Submit Request Answer Part J Give any common name for the following compound. Br CH3 If the compound has only the IUPAC name, enter no. 1-bromo-2-methylbenzene Submit Previous Answers Request Answer X Incorrect; Try Againarrow_forwardWrite the IUPAC name of the following compounds. Observe proper punctuations. Make sure that there are no spaces in between characters except those that have in their parent chain. Capitalize ONLY the first letter of the name. Also, don't use CIS/TRANS or E/Z in naming the compounds.arrow_forwardAdd the appropriate number of hydrogen atoms to the alkynes and give their IUPAC (systematic) names. Add the appropriate number of hydrogen atoms to IUPAC name: the alkyne. Select Draw Ringa More Eгese H Add the appropriate number of hydrogen atoms to IUPAC name: the alkyne. Select Draw Rings More Erese H -C- C =arrow_forward
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