BH3 CH3 OH 2 Н.Ог, NaOH CH3-CH-CH-CH3 A в CH3 CH2 CH2=C-CH2-CH3 CH3-C-CH2-CH3 C D CH3 CH3 CH3-C=CH- CH3 CH3- CH- CH=CH2

Q: Give the IUPAC name for each compound.

A: Rules for naming organic compound is as follows; Select the longest continuous carbon chain.…

Q: CH3 CH,CH2-C-CH,CH2 f. CH3 CH3 CH,CH,CH2-C-CH3 ČH3

A:

Q: CH3 HCI CH3 CH3 CH3-CH-OH ZnCl2 CH3-CH-CI CH3-C=0 BCD DCB

A:

Q: CH2-CH3 CH3 -C- chz CH3 H -CH3 CH3 Pel4 ce CHS Heas PBY3 BY L 7 CH3 1Naon

A: Rules of IUPAC nomenclature First, we have to find the longest carbon chain that is continuous.…

Q: + 2H2 H20 > B Na H3C-C: EC-CH3 + 1H2 A + Cl2 NH3(1) A H20 → B H2SO4 -c=c-CH3 + H2 Lindlar H,O H3C-C…

A: Hydrogenation is process of adding hydrogen across the unsaturated bond

Q: Are the following compounds primary, secondary, or tertiary?

A: a) The compound is tertiary, because the functional group bromine is attached to a tertiary carbon…

Q: What is each compound’s systematic name?

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

Q: 1. CH3-C=CH2 CH3-CHz- CH CH; 2. CH3 - CH2 - C=CCH2 -CH; 3. (CH:),CHC CCH(CH3)2

A: Note: Since you have posted a  question with sub-parts , we are entitled to answer the first three…

Q: O CH3 - CH2 - CH2 - CH2 - CH2- CH = CH- CH3 %3D O CH3 - CH2 - CH = CH- CH2-CH= CHz-CH3 3 H, C- CHz -…

A:

Q: a. H3C-CH2-NH-C-H IUPAC H3C-CH2-NH-ĉ-H Common H3C-CH-CH2-CH2-CH2-C-0-CH3 b. Br IUPAC…

A: (a)  IUPAC name : N-Ethylmethanamide Common name : N-Ethyl formamide     (b)  IUPAC name :…

Q: 1. CH:-CH C-OH OH 2. CH:- CH-CH2-C-C CH: CH3 -C-CH2-CH2-C-OH CH: CI CH3-CH2-C CH2-C-ÖH ČI C-OH

A: IUPAC is a naming system by which we give a particular name to a compound. And this is  stand fòr…

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

A: Nucleophiles are the electron rich species and it can share at least a pair of electron.…

Q: 1. CH2-CH2 -МgBr 2. H3O* OH OH (a) CH-CH3 (b) -CH2-CH2 (с) CH-CH2 ОН (d) -CH2-CH-CH2 (e) -CH2

A: Given  Reactant =  PhMgBr and Epoxide  Product   = ?

Q: a.) H- C = C-H CH3 - C=C- CH2-CHz -CH2-CH3 b.) CH3 - C Hz- CH2- OH H3c-C三c-H C.) CH= CH A CH3 -…

A: According to our policy we should solve  one question ( if subparts presentthen first three subpart…

Q: CH;CH2- N-CH,CH3 + HCl - (21) CH,CH3 (22) || ethanol H;C-C- CH=CH, + HN(CH,CH3)2 CI (23) Br 1. ΗΝΟ ,…

A:

Q: CH2-0-C-(CH2)14CH3 %3D CH-O-C-(CH2),CH=CH(CH2},CH3 3 NaOH ČH2-0-C-(CH2)e(CH2CH=CH)2{CH2)4CH3

A: Triglycerides are esters of fatty acids and are formed by combining fatty acids with glycerol. When…

Q: CH3 CH3-CH2-C-CH2-C-CH2CH3 ČH3 b) c) CH3 CH3-CH2-C HO- | CH3 d) CH3 CH3 он CH3 CH3-C-OH…

A:

Q: CH3-SH A 6 CH3 -CH=CH -CH2-CH3 OH C C CH3 -CH -CH3 レ C3-CHz -CH E CH3 -CH2-0-CH2では

A:

Q: CH3-C I -CH3 1. ВН:/THF CH3-CH2-CH2-C-H or 2. ОН, Н,О2, Н,о CH3-CH2-C CH | II

A:

Q: (2 CH3 H;C-CH,-C-CH3 NH2 CH3 CH3 H3C-CH2-C-COOH NH2 H3C-CH2-C-C,H5 H3C-CH2-CH-CH3 NH2 NH2 6. 8, OH…

A: Asymmetric carbon - It is that carbon atom which is attached to four different groups or different…

Q: CH3-CH2-CH2-NH3* CI + NaOH etq CH3 ow or mi en CI CH3- N*-H КОН + CH3

A: In the reactions given, there is a ammonium salt of which is a weak acid which is reacting with…

Q: Which of the following compounds has an asymmetric center?

A: Asymmetric centre is a molecule having a special arrangement of ligands which is not superiposable…

Q: (d) –CH3, –CH2CH3, -CH2CH2OH, -CCH3 (e) -СH3CH2, -сN, -CH-NH2, -CH2Br (f) -CH=CH2, -CH2CH3,…

A:

Q: H2NNH2, ОH (d) CH3-CH2-C-CH2-CH3 1. LIAIH4 (u) 2. Hзо* H2NNH2, OH (w) Нeat

A: In presence of NH2NH2 / OH- Aldehyde and ketones undergo Wolff Kishner reduction and we get Alkane…

Q: OH CH,CHCH,CC=CH CH, CH3 Çi C1 CH 3-CH-CH 2-CH-C-CH-CH 2-CH2-OH tH-CH, C1 CH3-CH,-CH;-CH2-NH,

A:

Q: b. CH3 CH2 -N-CH,-C- || -CH,-C-N-CH-C- -N-CH-C-N- H OH OH с. но OH но- OH 0-CH;CH2-0 0-CH;CH-O

A: Following monomers condensed to form the given polymers with removal of water molecule .

Q: 12, CCI4 CH2-0-C-(CH2)7-CH=CH-(CH2)5CH3 H2, Pt CH-O-C-(CH2)16CH3 3 NaОH ČH2-0-C-(CH2)14CH3 H30*

A: The given reactions are :

Q: 1. CH&CH(OH)CH=C(CH3)CH,CHs 2. CH,CH-C(CH3)CH2CH(-O) 3. CH;CH2CH(NH2)CH(CH2CH;)CH2CH2CH3 4. CH3 5.

A:

Q: CH3-C=CH2 CH3-CHz- CH CH3 CH3- CH2 - C=CCH2 -CH3 (CH:)>CHC-CCH(CH3)2 (CH3)»CCH=CCH(CH3)2 CH3- CH2…

A:

Q: 1. CH3-C=CH2 CH3-CH- CH CH3 2. CH3 - CH2 - C=CCH2 -CH; 3. (CH)»CHC CCH(CH)a 4. (CH3):CCH=CCH(CHs)2…

A: Answer  Common name :- old derived and popular name called Common…

Q: What stereoisomers are obtained from each of the following reactions?

A: Since you have posted multiple sub-parts, we are entitled to answer the first three only.

Q: 2. 3. CH3 CH3 CH2 CH3CH2C=CHCH3 CH3-CH-C- CH3 CH-CH-CH-CH-CH3 Br ČH3 OH 4. 5. 6. OH CH; 0 CH3 H;C…

A: In this question, we have to find out the correct answer of given problem by the help of the…

Q: CH3 CH,- -CH, h CH2-CH3 H,C-CH;- -CH2-CH3 ČH,-CH, b0

A: Question - g The long carbon chain contains 3 carbon atoms and two methyl groups at 2 position,…

Q: ) O=C-CH2-CH Jo-CH2-CH2 C=C-CH₂-CH₂ C-CH₂=CH

A: The partial structure for a doublet integrating to 2H at 2.3 ppm is

Q: CH3 f RR'CHОН + О-S `CH3 DCC, H* » ?

A: Dimethyl sulfoxide first attacks carboiimide which allows the added alcohol to attack positively…

Q: CH,CH, CHg (b) CH, CH,CHg (c) HgC CH3 CH;CH,CHCH,CH,CHCH3 CH;CH-CH;CHCH>ÇCH3 CH3C-CCH,CH;CH3 CH3 HgC…

A: Please find the file attached for explanation

Q: H;C-H,C' i) + Ph;P=CH-CH3 ii) (CH3),CHCH2CI AICI; iii) H2SO4

A: Given

Q: a) b) c) --- CH-CECH CH₂-CH-CH CH₂ I C=CH CH₂-CH-CH₂ CH₂ ट CH + 2Br₂ + 1Br₂ + 2HCI

A: Alkyne + 2 moles of Br2 Alkyne + Br2 Alkyne + 2HCl

Q: a. CH;(CH2)4I, CH3(CH2)5I, CH3(CH2)çI b. CH3CH¿CH;NH2, (CH3);N, CH3CH¿CH,CH3 c. (CH3);COC(CH)a,…

A: Boiling point of a chemical compound is the temperature at which vapor pressure of a compound…

Q: Draw curved arrows to show the movement of the electrons as one (or more)bond breaks and another…

A: a. Carbon-carbon π bond undergoes homolytic cleavage. Among the two electrons of carbon carbon π…

Q: CH3 CH3 CH3 NaOCH3 H CH,0CH CH3 CH;0 CH2CH3 CH2CH3 Br SN2 H VWX XWV O VWX O XwV

A: The SN2 reaction is a nucleophilic substitution reaction. It is a one-step reaction where the…

Q: H-C-CH2-CH3 H3C- C-O-CH2-CH3 H3C-CH2-OH H3C-NH-CH2-CH3 H3C- -CH2-CH3 H3C-C-H Br H3C-CH2-CH2-C-OH…

A: The functional group is the specific moieties in the molecule that are responsible for all the…

Q: CH3 HCI CH3 CH3 CH3-CH-OH ZnCl, CH3-CH-CI CH3-C=0 BCD DCB BCD DCB

A: Lucas reagent: The mixture of HCl and ZnCl2 is a Lucas reagent which is used for the test of…

Q: CH2-CH-CH=C-CH2, CH₂ CH3-CH2-CH-OH CH3-CH2-CH2 OH OH CH, CCH, CH, CH3 H₂SO4 140C KMnO₂ H₂SO4 180C…

A: We have to give the IUPAC name of the products of the given reactions.

Q: Which species in each pair is more stable?

A: “Since you have posted a question with multiple sub-parts, we will solve first three subparts for…

Q: Give the complete IUPAC name for each of the following compounds:

A: IUPAC name of (a) Butan-2-ol  IUPAC name of (b) 2-iodo-3,3-dimethylpentan-2-ol  IUPAC name of (c)…

Q: Explain why a random copolymer is obtained when 3,3-dimethyl-1-butene undergoes cationic…

A: The intermediate for the cationic polymerization of 3,3-dimethyl-1-butene is the carbocation which…

Q: H2N-CHC-OH CH2 H2N-CHC-OH CH2 H2N-CHC-OH CH2 C=0 N. OH NH

A: Amino acids contain carboxylic acid and an amine functional group on the same carbon atom. Amino…

Q: How can 1H NMR distinguish between the compounds in each of the following pairs?

A: NOTE: Since, we only answer upto three sub-parts, we'll answer the first 3. Please resubmit the…

Introduction to Organic Chemistry

The field of chemistry which deals with the studies of reactions, structures, and properties of organic compounds that comprise carbon bonded through covalent bonding is organic chemistry. The studies regarding the structure of organic compounds could be determined with the help of structural formulas. In order to know about the behavior of organic compounds, a study on the properties has to be done. Both physical properties and chemical properties, the origin of chemical reactivity come under the study regarding the properties of organic compounds. The chemical preparation of polymers, drugs, natural products, and the study of separate organic molecules in the lab come under the study of organic reactions.

Vinyl Group

Vinyl group is the name given to the functional group of -CH=CH2. It can be seen as an ethene molecule with one less hydrogen in number. Hence it is also called as ethenyl group at times.  

Straight Chain Hydrocarbons

The requirement to identify each compound needs a richer number of words than informative prefixes like n and iso. The identification of organic molecules is made easier by the use of systematic nomenclature schemes. The organic chemistry nomenclature has two types: traditional and systematic. Common names arise in many forms, but share the characteristic that a link through name and form is unnecessary. The name that matches a certain structure clearly must be remembered as knowing a person's name. In contrast, systemic names, including an overall common set of laws, are locked specifically to the chemical structure. 

Unsaturated Hydrocarbon

Following are few examples of alkenes with their general molecular as well as their structural formulas: 

Conjugated Compounds in Organic Chemistry

The delocalization of electrons in a molecule is called conjugation in organic chemistry. This delocalisation process of electrons leads to the shortenings or elongations of chemical bonds, but at the same time it causes changes in the chemical properties in conjugated molecules as compared to the non-conjugated ones. For example, conjugated molecules absorb light at longer wavelengths. 

Alpha Carbon And Alpha Protons

The carbon directly attached to the functional group in an organic molecule is referred to as the alpha carbon and the hydrogen attached to an alpha carbon are termed as the alpha hydrogens or alpha protons. These alpha carbon atoms and alpha hydrogen atoms are of importance because they undergo certain characteristic reactions in organic chemistry.