Q: Rank the carbocation compounds below from most stable to least stable.
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Q: CH; +CH CH; I II III IV
A: We have to rank the following given carbocation in order of increasing stability as follows in step…
Q: Rank the following according to DECREASING reactivity towards SN2: H 19 CH₂ CH3 1st (most reactive)…
A: Given compounds are : Rank the following according to decreasing reactivity towards SN2 ? SN2 =…
Q: Rank the following carbocations in terms of their energy. A В
A: Carbocation are organic species formed from alkane when hydrogen is lost thus carbon bear positive…
Q: Which of the following carbocations (A or B) is more stable? Explain your choice. ö-CH2 -Ñ-CH2 A
A: The carbocations (A or B) that is more stable has to be given and reason has to be explained.
Q: CH2 CH А. C. D. H IU-UH B.
A: The stablity of carbocation depends upon number of hyperconjugation structures, which depends on…
Q: Explain why1-bromobicyclo [2.2.2] octane is not likely to undergo an SN1 or an Sn2 substitution…
A: No SN1 or SN2 reaction is likely to undergo for 1-bromobicyclo[2,2,2] octane . In the SN1 reaction,…
Q: H3C. CH3 .CH3 H H3C. CH2 H3C @ CH3
A: Tertiary carbocation is more stable than secondary carbocation which is more stable than primary…
Q: fonowing cо ounds using H3C. CH3 HC CH3 CH3 CH3 CH2 H3C „CH2 CH ÇH HC CH3 H3C CH2 CH H3C-HC CH3 H2C.…
A: The IUPAC name of an alkane is determined in the following manner: The longest carbon chain is…
Q: c. Hint: I'd sure use Newman projections or a model kit to predict this product! Br Ph CH3 (solvent)
A: Biomolecular elimination (E2) reaction:E2 reaction involves a one-step mechanism in which…
Q: Reagents Available a. CH2=CHCH2CI, AICI3 b. CH2Br2, OH c. CH3CH2COCI, AICI3 d. H2, Pt e. NBS, CCI4…
A: The given compound can be synthesized from catechol (1,2-benzenediol) using the reagents mentioned.
Q: Rank the following carbocations, from least stable (left) to most stable (right). i. ii. ii. O i. <…
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Q: Rank the following carbocations in order of increasing amounts of hyperconjugation. The first in…
A: The amount of hyperconjugation depends upon the number of hydrogen atoms on the adjacent carbon to…
Q: Classify the following carbocations as primary, secondary, tertiary, methyl, or vinyl carbocations…
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Q: f. g. h. i.
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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: 3. In each pair, circle the species that is more stable. OH2 OH2
A: In the first pair, the second structure is more stable. The stability of the carbonation depends on…
Q: Question 8 Rank the following carbocations from most stable to least stable: II II O III >I> II OI>…
A: Given that, Three carbocations have been given,we have to find out order of stability?
Q: For each pair of structures in i-v, select the one that is more stable. i. [ Select ]
A: The stability of the product depends upon various factors. Some of them include: Less hindered…
Q: 3) Draw the ECSF structures of (CH3)3CO® (tert-butoxide ion) and CH3O® (methoxide ion). Why is…
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Q: 4.9 4.15 4.10 1. NaH 2. CH3Br KMNO4, HO- Heat, H20 H2SO4 SOCI2 pyridine POCI3 но 4.14 4.11 pyridine…
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Q: Determine major product of the rxn Ag20 H20 (CH3)2CHCH2N(CH2CH3)2 CH31 heat products (a)…
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Q: Reagents Available g. CO, HCI, CUCI/AICI3 h. CH3CH2CH2COCI, AICI3 a. CH2=CHCH,CI, AICI3 b. CH2Br2,…
A: The answer is as follows:
Q: A In each blank, type the letter of the more stable alkene in each pair (type A or B). A blank 1…
A: The stability of an alkene depends on the substituted groups around the double bond. It will also…
Q: Which compound(s) is(are) secondary haloalkane(s)? H CH3 CH3 CH3-C CH3 CH3-C CI CH3-CH2-CH2 Br…
A: Secondary haloalkanes are those compounds in which halogen attached to carbon is further atteched…
Q: Classify the following carbocations as 1o, 2o, or 3o and b) rank the following carbocations in order…
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Q: Rank the molecules below from least stable to most stable
A: we have been asked the stability of given ring structure
Q: what order would this 3 step EAS reaction take place?
A: Benzene undergoes electrophilic substitution reaction by the reaction with any electrophilic reagent…
Q: Rank the following carbocations in order of decreasing stability. Most stable
A: Carbocations are electron-deficient species that are formed by the removal of a hydrogen atom from…
Q: 6. Rank each set as indicated. No explanation required a) Rank bases in order of increasing…
A: To rank rhe the given compound according to nature given
Q: Draw the energy verses course of rx curve (energy diagram) for the reaction 4 PH3 + 2 H2 + 9 02 5 2…
A: To draw the energy diagram , we would check what type of reaction is it . As reaction is at…
Q: Rank the following carbocations in order of decreasing stability (most → least): CH₂CHCH₂…
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Q: 1. Sort the following molecules into the quadrant in the chart shown below that best describes them.…
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Q: Br K* OC(CH)3 K* OC(CH); Br cis trans
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Q: Determine major product of the rxn CH3 -CH = CH – CH2 -CO2H- → (X) (major); Product (X) is : (a) CH3…
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Q: Rank the following carbocations in decreasing stability (most stable to least stable). [Note: your…
A: Carbocations are carbon ions which have a positive charge on it and its hybridization is sp2.
Q: 1. Sort the following molecules into the quadrant in the chart shown below that best describes them.…
A: Nucleophiles are the chemical compounds which are electron rich and provide electron density to…
Q: H. Br C6 CI H E2 C2 H. CI Br 1) which one is product? 2) which one is least likely? 2.
A: Introduction: Elimination reaction: Elimination reaction is a reaction in which substituent gets…
Q: The most stable carbocation a
A: A carbocation is a planar molecule in which a carbon atom has a positive charge and three bonds.
Q: + Class: Stability ranking: ||
A: A electron deficient species contains three bonds with positive charge on carbon atom is known as…
Q: "NH2 CH3BR 2H2/Pt H3C-c=CH → A В C
A: Sodium Amide is used as a strong base. The methyl bromide gives the possibility of a nucleophilic…
Q: 2. Rank the following anions from most to least stable. a. b. d.
A: . Stability of anion depends upon the following factor :-a Resonance stabilize the anion .b Lower…
Q: CH3 H (+) H;C-C-CH3 H,C-g-CH, CH3 H3C-CH2 А. С. D. B.
A: In this question, we will Select the most stable carbocation. You can see details explanation and…
Q: Which of the following is the most effective way to stabilize carbocations? a. Zaitzev's rule O b.…
A: Carbocation stablized by electron donating group or resonance when positive charge is in conjugation…
Q: Arrange the following groups in the order of increasing priority (lowest priority to highest…
A: Polar covalent bond:The covalent bond is formed by the sharing of electrons between the atoms. If…
Q: 1. Which is more reactive towards Nu-? 1. Н-с-н vs -CH2CHO 2. H2N- -СНО vs CHO -СНО Vs -COCH3 3.
A: Nucleophile is an electron donating species to form a chemical bond which attack on electron…
Q: (i) increasing solubility in water. (CH3),CHCH,OH CH;CH,CH,CH,OH CH;CH,CH,Br CH;CH,OCH3 (a) (b) (d)…
A: The sequences are as follows:
Q: Match each alkene to its heat of hydrogenation. Alkenes: 3-methylbut-1-ene, 2-methylbut-1-ene,…
A: The structures of given compound are shown below:
Q: Which carbocation is more stable? CH3C+H2 or H2C=C+H
A: The more stable carbocation is to be identified: CH3C+H2 or H2C=C+H.
Q: 4. Why do we have to keep Fehling's A separate with Fehling's B?
A: The question is based on the concept of qualitative analysis. We have to explain the reason for…
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- Hello, thank you this was very helpful. However, i still dont completly understnad how to determin and explain why the isomer of B is the major product. Could you explain this in a differnt way?do not fully undsertand the slide，need further explanation. what does it means by the additive effect of two group？which two group ？？why OH is a more powerful activator than CH3？ meta rarely take please because it is too hindered？why too hindered？Too hindered in EAS or which reaction？why？？I am confused.( give clear handwritten dont copy previous ans )