Derive an IUPAC name for the following (cyclo)alkenes: (Do not use cis/trans in your names. Use only the (E)/(Z) designations for double bond stereochemistry. It is not necessary to use italics in writing compound names.) 1: 2:
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Q: Derive an IUPAC name for the following (cyclo)alkenes: (Do not use cis/trans in your names. Use only…
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Q: CH3 H3C-CH H H3C-CH-CH2-CH2-CH-CH2-CH3 ČH2OH H CH3 а. b.
A: Interpretation: The IUPAC name for the following compounds are to be provided. a) b)
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- Derive an IUPAC name for the following (cyclo)alkenes. (Do not use cis/trans in your names. Use only the (E)/(Z) designations for double bond stereochemistry. It is not necessary to use italics in writing compound names.) (a) (b) Br C1 -ClDerive an IUPAC name for the following (cyclo)alkenes. (Do not use cis/trans in your names. Use only the (E)/(Z) designations for double bond stereochemistry. It is not necessary to use italics in writing compound names.) (a) (b) my XName the alkene using the 1993 IUPAC convention. Be sure to indicate stereochemistry and use hyphens (-) not endashes (-). H₂C-CH3 H H3C H₂C-HC C=C H CH3
- Draw a structural formula for the alkene you would use to prepare the alcohol shown by hydroboration/oxidation. OH AFFIL CH3 CH3 H • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one. Sn [F ? ChemDoodleProvide an IUPAC name for each of the compounds shown. (Specify (E)/(Z) stereochemistry, if relevant, for straight chain alkenes only. Pay attention to commas, dashes, etc.) CH3 CH3 ČH3 (H3C)3C H C=C C(CH3)37.33 a-Farnesene is a constituent of the natural wax found on apples. What is its IUPAC name, including stereochemistry? 7.34 Menthene, a hydrocarbon found in mint plants, has the systematic name 1-isopropyl-4-methylcyclohexene. Draw its structure. 7.35 Draw and name the six alkene isomers, C5H1o, including E,Z isomers. a-Famesene 8.22 Name the following alkenes, and predict the products of their reaction with (1) meta-chloroperoxybenzoic acid, (2) KMnO4 in aqueous acid, and (3) 03, followed by Zn in acetic acid: (a) (b) (a) 8.23 Draw the structures of alkenes that would yield the following alcohols on hydration (red = O). Tell in each case whether you would use hydroboration- oxidation or oxymercuration-demercuration. (b)
- When (1-bromoethyl)cyclopentane is heated in water for an extended period of time, SIX products result: three alcohols and three alkenes. Draw the three alcoholsDraw a structural formula for the alkene you would use to prepare the alcohol shown by hydroboration/oxidation. -CHCH3 ОН • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one.Name the alkene below. Use ONLY E/Z designators to indicate stereochemistry. H CH3 H3C C=C H2C=CHCHÇH H ČH3
- Provide an IUPAC name for each of the compounds shown. (Specify (E)/(Z) stereochemistry, if relevant, for straight chain alkenes only. Pay attention to commas, dashes, etc.) Br. H C=C CH3 H₂C-CH₂ C=C H CHCH(CH3)2 CH3Q1: Give IUPAC name for the following structures. (five only) Br H,C CH3 но ČI -OH Q2: draw the structure of each of the following compounds 1) 1,2-Dibromo l-3-cyclooctdiene 2) cyclopentyne 3) butylcylopentane 4) tetrachloromethane 5) Cis-2,3-dibromo-2-buteneWrite down the common (not IUPAC) names of the organic molecules that would be released if this molecule were hydrolyzed: CH2−O−C—(CH2);–CH=CH–CH2–CH=CH—(CH2)4—CH3 CH-O-C-(CH2)14-CH3 O 11 CH2−O−C— (CH2)14 — CH3 Separate each name with a comma. You will find useful information in the ALEKS Data resource. 1 010 Continue O a X 000 Y F8 F9 Submi