Most Stable Least Stable Answer Bank 1,c–CH2 CH3 H CH3 H3C CH3 H3C° CH3

Q: Hemiacetal Аcetal Other Answer Bank H3C CH3 CH3 CH3 ОН ОСНЗ CH2 CH2 OH CH3 CH;CHOCH2 OH CH;OÇOCH3…

A: The separation of given compounds as hemiacetal, acetal and other is given in attached image.

Q: (a) H H-C-C=C-とーとーとーH H. (6) H-C-H H H-C-H エ-U-エ %3D - =

A: a) The compound given is  Hence the functional group in the above compound is alkene i.e C=C. And…

Q: CH-CH3 CH,CH, CH,CH3 CH CH,CH, H. H. H. CH3 -CH3 H. H. H. H' H. H H ČH3 IV H.

A: Answer- Conformarion in which both the bulkier group are at maximum distance or at opposite side…

Q: -CH3 FeBr3 + Br2 CH3 -CH3 -CH3 Br Br Br III I II (d) I and III but not II (e) II and III only (a)…

A: The given reagent is a brominating agent where tribromo iron is an oxidising agent which forms the…

Q: Select the best answer. но 1.) SOCI, 2.) AICI3 3.) H2, Pd/C CH3 a) 1.) b.) 1.) c.) 1.) 2) 2) 2) CH3…

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Q: H H HH H |||| | H–C-C=C-C-C-H | H H H

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Q: Q3// Give the nonmacular of the following compound: Br CH3CH-CH-CH3 Br CH3 `NO2 -CH-CH3 CH CH CH ҫH2…

A: The IUPAC names of the following compounds are as follows:

Q: H,C HN-CH2 CH3 H2 C HC H2 CI H3C H2 CH.

A: The reaction is a nucleophilic substitution reaction.

Q: CH2 CH2 H3C ČH3 е. CH2 CH2 CH2 CH2 H3C ČH3 f. H3C CH CH2 CH3 ČH3 ČH3

A: There are many functional groups in organic chemistry.  And it is very difficult to name any…

Q: HOCH2CH2OH H* Br2 (excess) HO. 7. NaOCH3 CH3OH C6H5 5. 6.

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Q: Give the IUPAC name for each compound.

A: IUPAC name has to be given below.

Q: H2 .C CH H2 .C HCH2 C' CH3 C' H2 H3C. H2 H3C H3C to CH3 CH3 H3C~, CH2 H2 CH H CH3 H3C. C. H2 H2 HC…

A: IUPAC rules to be followed:- 1) select the longest possible carbon chain. 2) give lowest possible…

Q: Н-Н H-CI 436 kJ/mol С-Н 413 kJ/mol C=C 614 kJ/mol 431 kJ/mol C-C 348 kJ/mol 839 kJ/mol 567 kJ/mol…

A: The reaction taking place is given as, => H-H + Cl-Cl -----> H-Cl + H-Cl

Q: H H H H 2. H-C-C-C = C - H H H H

A: The given compound contains a carbon-carbon double bond, hence it is an alkene. The IUPAC name of an…

Q: CH3 CH2CH3 cHz CHz をHz NOZ 2. 3. cHzい。 り CH3 RCHICH2 CH3 2.

A: Order of stability of carbocations are :  1) b>a>d>c  2) d>a>c>b 3)…

Q: F3NH4* Ct. lat Hz-C-CH2-C00. a* F3-C-CH2-CO0. H;NH Ch. a* Clo,

A: As we know,  Acids and acidic salts have pH less than 7. Bases and basic salts have pH greater than…

Q: guur 39 t (s) II CH3-C-NH-CH3 A CH3-C-CI CH3-NH2 HCI II CH3-C-0-CH3 + H* B CH-С—он + CHз-ОН H20 OH…

A: Energy diagram

Q: d. H3C KMNO4 ОН H3C е. OH CH3 KMNO, f. HI H3C-0–CH2 CH3

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Q: C2H5OH (CH3)з С - Br (CH)з С - О - Н + H2O (CH)з С - ОС2Нs + CHa %3D C(CH3)2

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Q: CI Your answer SH H3C, CH3

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Q: H3C. \'C=N CI HO'CH2OH H \'H CH2CH3 CH,CH, H2NH2C

A: R-S Configuration CIP Rule: 1) If the atoms are different then given priority on the basis of no.…

Q: CH3 CH2OH CEN a. с. Br -ОН C. CH3 CH2NH2 b. CI OCH3 d. HOCH2 Br CI CH2NH2

A: In the letter E, the horizontal strokes are all on the same side; in the E isomer, the higher…

Q: H н H.C Н CH₂ I н CH₂ i Н Н H. C на H Ï CH₂ H H Н | Н H

A: Amino Acid  Amino acid are white crystalline solid . It contain both basic amino group(-NH2) and…

Q: Draw a stepwise mechanism for the following reaction.

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Q: CH3 CI CH(CH32 А. DBN CH(CH3)2 "CH3 CH(CH32 CH3 CI CH(CH32 DBN CH3 CH3 CH(CH3)2 CH(CH,)2 B.

A: It is an second order elimination reaction. At first we have to draw the stable chair configaration.…

Q: CH3 CH3 CH3 Н. H. H. Н. H H. H H CH3 I-

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Q: 2. Draw the condensed formula for н— с — н %3D H H нн H HHH IIII H-C-C-C-C-H н— с — с - с — н -…

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Q: а. но H онн || | | H3N-C-C-N-CH-C-Ń-C-Coo CH2 HC-OH ČH3 NH2 b. нон онн | | H3Ñ-c-C-N-CH-C-N-C-coo |…

A: Tripeptide is formed by three amino acids. The amino acids attached by a peptide bond. Three-letter…

Q: (g) (e) -OH-CH=CH-_1_C1₂ CH₂-C OH CH₂ CH₂ HCUN O Heat KMnO4, hot H* 1. NaBH4 2. H₂O

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Q: H. H. Brll CI- Br CH3 CI ČH3

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Q: Which reacon ve H3C. CH3 Br CH3 Br H3C. CH3 ČH3 Br H3C. ČH3

A: Iodide ion is a strong nucleophile so it gives Sn2 reaction. So 1-degree alkyl halide will easily…

Q: CH3 CH2 CH3 ČH ČH H3C. CH CH CH3 ČH3 ČH3 а. Br CH2-CH CH3 b.H3C CH3 H3C-C- CI ČH3 С. CH2 CH2 ČH CH…

A: IUPAC name of all the compounds are given below

Q: True or false  Kc= [NH3]2 /[N2]2[H2]3 for N2+3H2 2NH3

A: The equilibrium constant expressed in terms of concentration Kc explains the relationship between…

Q: please I want an answer q1 [ b. ii]

A: The answer of the above question is given in following steps

Q: (i), (ii), [ii), [iv], [v], [highest] and [lowest] I. CH;NH2 CH;CH;CH3 „CH3 II. CH,OH II CHCCH, V.

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Q: H. Br Br H H3C- FH OH CH3 Br Br F Br Br CH3 CH3 H- CI H- CI H- CI H- CH3 CH3 CH3 CH3 CI OH -H- CI H-…

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Q: your answer. Br + H,0 a) or ii. + H,0 i. + H,O (1.0 M) b) or ii. + H,0 (2.0 M) + CH,CH,OH Br or +…

A: The SN1 product depends on the stability of carbocation (degree of Carbocation),Attacking power of…

Q: NAOME MeoH CH3 Br

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Q: CH3 CH3 B C A CH3 H Ph;P CH3 Ph3P CH,CH(CH3)2 Ph,P CH(CH3)2 D E F

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Q: ghlige CH3 CH2CH3 CH3CHCHCH3 sto. (CH3)3C harno CH2CH3 romp

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Q: H. (CH3),CBr AIBT3

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Q: Он H H OH H-C- CH3 H он H3C- С—н H ČH3 H I-

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Q: NO2 NC a L• NacN → H NO3|H2 80y ho NacN → CH3 Coal Al3 → HNO3 l Hz S04 H20 CH3 COCl IMid3 → HCN…

A: Aromatic halide does not give a nucleophilic substitution reaction. If we add electron withdrawing…

Q: CH3 CH3 a.) HO ce b.) -CH3 NH C Hy- NCH2CH3 c.) CHzCHz CHz CH CHz (Hz NH2 d.) d.) CH7-C- CH2 -CH e)…

A: Functional group are written in alphabetical order in naming.

Q: CH3 H2 H3C-C-c-C- он H2 -C-CH3 اجابتك OH H3C он اجابتك

A: The IUPAC name of the given compounds has to be determined. a) b)

Q: b. CH3 CH3-C-(CH2);CH3 2502 spark CO2 + H2O CH3

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Q: CH3 H3C CH3 CH3 CH3 H3C -CH3 H3C `CH3 CI CI H,C. CH3 ÇH3 Br H3C CH3 -CH3 CI H3C H3C H3C `CH3 Br F CI…

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Q: А. B. C. D. HO w.. H3C CH3 CH₂ H CH3 CH3 CH3 CH3 HC3 CH3 HC3 CH3 Ž HC3 CH3 OH OH om CH3

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Q: H) H2C=HC. COOH CH,OH H3C Configuration:_ Name: 1). H3C CH3 CH2CH3 H;CH2C Configuration:_ Name: J).…

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Electronic Effects

The effect of electrons that are located in the chemical bonds within the atoms of the molecule is termed an electronic effect. The electronic effect is also explained as the effect through which the reactivity of the compound in one portion is controlled by the electron repulsion or attraction producing in another portion of the molecule.

Drawing Resonance Forms

In organic chemistry, resonance may be a mental exercise that illustrates the delocalization of electrons inside molecules within the valence bond theory of octet bonding. It entails creating several Lewis structures that, when combined, reflect the molecule's entire electronic structure. One Lewis diagram cannot explain the bonding (lone pair, double bond, octet) elaborately. A hybrid describes a combination of possible resonance structures that represents the entire delocalization of electrons within the molecule.

Using Molecular Structure To Predict Equilibrium

Equilibrium does not always imply an equal presence of reactants and products. This signifies that the reaction reaches a point when reactant and product quantities remain constant as the rate of forward and backward reaction is the same. Molecular structures of various compounds can help in predicting equilibrium.