7. What is the systematic (IUPAC) name of the following structures? CH3 H3C CH2-CH2-CH3 .CH CH2 CH-CH-CH2-CH3 H3C CH CH3 H3C-CH H2C-CH3 ČH3 CH3 CH3 CH3 H3C-CH2 CH-CH3 CH3CH2CH-CH-CH-CH2ČH-CH3 ČH2CH3 H2C-CH2 CH3

Q: See attachment

A: Geometrical isomerism:Geometric isomerism is a form of isomerism in which two substances have the…

Q: 1. Give IUPAC names fro the following alkyl halides: (a) CH3CH2CH2CH2I CH3 CH3CHCH2CH2CI (b| (c) CH3…

A: Since you have posted a question with multiple subparts, we will solve the first three subparts for…

Q: Give IUPAC names for the following compounds: (а) „CH3 (b) H3C CH3 (c) CH3 H- "CH3 (d) CH3 (e) CH3…

A: IUPAC name of the following compounds have to be given below, (a) (b) (c) (d) (e)

Q: Give a systematic or common name for each compound. a. CH,NHCH;CH,CH,CH3 e. (CgHs)2NH h. CH,CH3 NH2…

A: Hi, since you have posted questions that has multiple subparts. We will answer the first three…

Q: Which reagents lead to CI - O1. CH3CH2CI, AICI3 2. Cl2, AICI3 O1. Cl2, AICI3 2. CH3CH2CI, AICI3 1.…

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Q: A. Provide the IUPAC names for the following: ÇH3 CHCH,CH3 CH3 CH2CH3 CH3CHCH2CH2CH CH3 C=C H3C Hạc…

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Q: Give the IUPAC name of each alkyne. (a) CH3 CH3 (b) CH3 CH3CHC=CCHCH3 HC=CCCH3 CH3 (c) CH3 (d) CH3…

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Q: The most stable structure of trans-1-Bromo-3-methylcyclohexane is CH3 Br ZCH3 Br. ČH3 Br ČH3 Br

A: Most stable  structure  trans -1 bromo -3-methyl cyclohexane  on the basis of angel strain energy.

Q: 1. Give the IUPAC name of each alkene. H3C CH3 H2C=CHĊHCH3 (а) (b) CH3 CH3CH2CH=ĊCH2CH3 CH3 Onl (с)…

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Q: . a.) Classify the following carbocations (1º, 2º, or 3º). b.) Encircle the carbocation/s that can…

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Q: CH3 H3C- CH CH CECH CH3 CH2 ČH3 CH3 5 CH2 H3C-CH-ĆH- CH2 CH3 ČH3 H3C- CH-CEC- CH -CH3 CH2 CH3 CH3

A: Answer : Naming of alkenes and alkyne : ★ Find the longest carbon chain that includes both carbons…

Q: Rank the following alkenes in order of increasing stability: CH,=C(CH3)CH,CH3, CH2=CHCH(CH3)2, and…

A: Stability of alkene is directly proportional to number of hyperconjugation structures and number of…

Q: 2. Arrange these carbocations in order of increasing stability. CH2 CH3 -CH3 C. b. a.

A: Stability of carbocation can be compared using hyperconjugation effect. Carbocations with having…

Q: Give the IUPAC name for each alkyne. a. CH;CH,CH(CH,)c=cCH,CH3 d. HC=C-CH(CH,CH3)CH,CH,CH3 g. CH3 e.…

A: IUPAC name is as follows

Q: Give the IUPAC name for each alkyne. a. CH,CH,CH(CH3)C=CCH,CH3 d. HC=C-CH(CH2CH3)CH,CH,CH3 g. CH3 e.…

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Q: 3. Give IUPAC names for the following alkanes: (a) CH3 (b) CH3 CH3ĊHCH2CH2CH3 CH3CH2CCH3 CH3 (c) H3Ç…

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Q: The expected product from the addition of HCl to CH3–CH2–CH=CH2 is? CH3-CH2-CH2-CH2CI…

A: There are many mechanisms in organic chemistry such as nucleophilic substitution, nucleophilic…

Q: Name the following alkenes: CH2CH3 CH3CHCH2CH2CH C=c H3C (a) CH3 (b) CH3 (c) CH2CH3 CHCH2CH3 CH3…

A: Answer:- This question is answered by using the simple concept of naming of alkenes using the simple…

Q: 1. Give IUPAC names for the following compounds: (a) (b) CH3 H2C=CHCHCCH3 CH3CH2CH=ĊCH2CH3 CH3 CH3…

A: 1. Sol :- Since you have asked multiple questions, we will solve the first question for you. If you…

Q: Which carbocation is the least stable? CH3 lo IV. CH;CCH2 I CH;CH2 II. CH3CHCH3 CH3 CH3 I CH3CO V.…

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Q: Name the following alkenes: (а) CH3 (b) CH3 CH2CH3 (c) CH;CHCH,CH,CH CHCH,CH3 C=C H3C CH3 C=C H3C H…

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Q: 2. What is the structural formula for 4-sec-butyl Octanal? а. b. CH2 `CH2 CH2 CH2 CH2 -CH2 CH2 HC CH…

A: In this given question, we have to find out the structural formula for given compound name by using…

Q: 1. Give the IUPAC name of the following: (a) CH3 (b) CH3 (c) H3C CH3 CH3CHCH2CH2CH3 CH3CH2CCH3…

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Q: Give IUPAC names for the following compounds: (a) H3C CH3 (b) CH3 H2C=CHCHCCH3 CH3CH2CH=CCH2CH3 ČH3…

A: Since you have posted multiple question, we will solve first one for you. To get remaining  solved…

Q: 3. Show how to bring about each conversion. CH3 (CH2)5C#C Na* (b) → CH3(CH2)5C=CCH2CH3 (a) (d)…

A: Terminal alkyne  on reaction with NaNH2 gives acetylide which on reaction with EtI gives internal…

Q: CH,CH,CH, CH3 C=C (CH32CH H. H. CH3 C=C C=C H,C CH,CH3 H CHCH,CH,CH3 CH3 CH3 CH3 C Which of the…

A: Stability of an alkene is governed by Saytzeff's rule. It says that more alkylated the alkene the…

Q: 8. +) Draw the structure of (2S,3S)-2-chloro-3-methylhexane. Use wedges and dashes (where…

A: Answer :

Q: CH,CH3 H2C•CH3 H3C-CEC-CH-CHCH3 CH3 H3C-CH CHC-CH2CH2CH2 CH3 CH3 CH,CH, -CH2CH3

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Q: Name the following alkynes: (а) CH3 CH3 (b) CH3 CH3CHC=CCHCH3 HC=CCCH3 CH3 (c) CH3 (d) CH3 CH3…

A: a.  Long chain : it is a 6-carbon long chain ,  Hex Functional group: Alkyn at C-3   --->  3-yne…

Q: 8. Give IUPAC names for the following compounds: (a) CI „Br (b) CH3 (c) NH2 CH2CH2CHCH3 Br (d) CI…

A: IUPAC nomenclature is used for naming organic compounds. Full form of IUPAC is international union…

Q: 2. Please give the order of reactivity of alkenes CH3-C=ç-CH3 CH; CH3 CH3-C=CH-CH3 CH3-CH=CH-H CH3 B…

A: With the increase in the number of alkyl groups attached to the double bonded carbons, electron…

Q: Determine major product of the rxn CH3 -CH = CH – CH2 -CO2H- → (X) (major); Product (X) is : (a) CH3…

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Q: 7. Which of the following is more stable? 8. Name the compound according to IUPAC nomenclature. (Use…

A: When the high priority bulky groups are on the opposite side of the double bond, the alkene is…

Q: What is the substitution product of the reaction of CH3CH(CH3)CH2(CH₂)2Br with OH-? A)…

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Q: CH3-CH2-CH2-c= CH3 I H,O (а) or CH3-CH2-CH2-CH2-C-CH3 H,SO4, HØSO4 CH3-CH2-CH2-CH2-C=CH II

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Q: 2-propan-2-yloxypropane H- CH3 -OCH2CH2CH3 CH3CH2CHSH 6. 4. 5. OH CHз SH CH3 LOCH3 CH,CCH2CHCH2CHCH3…

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Q: Which one of the following alkenes is the most stable? H3C CH3 H3C CH3 H3C CH2-CH3 ÇH3 C= H3C. CH2…

A: More substituted alkenes are more stbale.More substituted  alkenes can attain more hyperconjugation…

Q: Give the IUPAC name for each alkyne. a. CH,CH,CH(CH,)C=CCH,CH, d. HC=C-CH(CH2CH3)CH,CH,CH3 g. CH3 e.…

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Q: What is the IUPAC name for the compound below?  choices:…

A: While writing a IUPAC name first identify the parent chain. Write the substituents alphabetically.

Q: Draw curved arrows to show the movement of the electrons that result in formation of the given…

A: Since we only answer up to 3 sub-parts, we’ll answer the first 3. Please resubmit the question and…

Q: 11. Name the following alkenes: b. CH. CH2. a. H,C- CH2 H,C: CH CH2 CH3 `CH d. .CH. CH3 H;C. CH"…

A: Always give numbering from that side from where alkene get least numbering..

Q: Show how to bring about each conversion in good yield.

A: The given compound is acyl chloride. It reacts with NaCH(COOC2H5)2 and further undergoes hydrolysis…

Q: An alkene react with Ozone ozonolysis to form CH;CH;CHO and (CH3),CO. The 9. alkene could be. A…

A: 9. We have given that A) CH3CH=CHCH(CH3)         →2. S(CH3)21.O3  CH3CHO + (CH3)2CHCHO B)…

Q: CH2 H2C CH3 CH C-CH3 H2C CH ČH3 CH3-CH-CH3 CH2=CHCH2CH=CHCH2CHCH3 CH3 CH3 HÖCH2CH2CCH2CH2CH ČH3

A: Bond-line structure also called skeletal structure. In molecular structure the covalent bonds are in…

Q: An alkene react with Ozone ozonolysis to form CH3CH;CHO and (CH3);CO. The alkene could be. A CH;CH =…

A: Ozonolysis is the process of reaction of alkenes or alkynes with ozone which results in the…

Q: OCH3 CH3 CH3CCH3 CH3CH-0- ÓCH3 CH3 CH3 SCH3 -SCH3 CH3CH2CHCHCHSCHCH3 ČH3 ČH3 SH -CH3 `NO2

A:

Q: 3. Name the following orga a) CH:CH CH CH2 CH3CH2CH2CH2C-O-CH2CH CH3 CH.CH2CH CH2 b)…

A: NAMING OF ORGANIC COMPOUNDS.The naming of organic compounds is completed with the assistance of the…

Q: II CH3-CH2-CH2-CH Butanal CH3 CH3 CH2 CH3 0 II CH3-C-CH,– CH3 CH2-CH CH3-CH-CH CH2 =C- CH3 A B D

A: The structure that is not an isomer of butanal has to be determined.

Q: -CH3-CH-CH2-CH-CH2-CH-CH2- ČH3 CH3 What is the monomer used to prepare the above? Oa. CH2=CHCH3 Ob.…

A: In the above polymer we can see that the repeating unit is

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.