Hydrocarbon by Ruhul Amin (201-29-1646) - Saturday, 15 August 2020, 10:32 PM Number of replies: 7 Please Can anyone explain why it's.Stability of Carbocation: 3°>2°>1°(alkyle)>methyleCarbanion: methyle> 1°>2°>3°(alkyle)23(b) Permalink In reply to Ruhul Amin (201-29-1646) Re: Hydrocarbon by Popy Rani Sutradhar - Tuesday, 18 August 2020, 3:22 PM because -CH3 is electron providing group. and more the number of electron providing group more stable will be carbocation. therefore 3 degree carbocation is more stable. Tertiary carbocation possess minimum positive charge due to - (1) hyper conjugation (2) electron releasing inductive effect of alkyl group primary carbanions have only one alkyl group and the increase in electron density is less on the carbon atom. Hence it is more stable thansecondary or tertiary carbanions. ... (other atom is a more electronegative atom). Permalink Show parent In reply to Popy Rani Sutradhar Re: Hydrocarbon by Mehedi Hasan Rabbi - Tuesday, 18 August 2020, 6:58 PM Why carbanion is more stable than carbonation? Mehedi Hasan Rabbi ID:201-29-1700 Permalink Show parent In reply to Mehedi Hasan Rabbi Re: Hydrocarbon by Sanjida ahmed Emma 201-29-1711 - Tuesday, 18 August 2020, 7:33 PM reactivity determined by several factors: The inductive effect. Electronegative atoms adjacent to the charge will stabilize the charge; Hybridization of the charge-bearing atom. Permalink Show parent In reply to Mehedi Hasan Rabbi Re: Hydrocarbon by kamrul hasan sujon - Wednesday, 19 August 2020, 9:14 PM carbocation is more stable. let's take for example the ter-butyl carbocation (Ch3)3-C+ this charged ion is highly stabilized due to the presence of the three donor methly groups that donate electrons, and hence largely stabilize the positive charge. On the other hand the tert-butyl carbanion (CH3)3-C- would be less stabilized and more reactive than its positive catine since The negatively charged carbon atom in carbanion is sp3 hybridized. Therefore, it has a tetrahedral structure. Three of the four sp3 hybridized orbitals form 3s-bonds with hydrogen or carbon atom of the alkyl group. The fourth sp3 hybrid orbital contains the lone pair of electrons.This would cause to bring the reactivity to this ion and makes it act as a free radicals. ID:201-29-1686 Section :23(A) Permalink Show parent In reply to Ruhul Amin (201-29-1646) Re: Hydrocarbon by Kazi Julfiker - Sunday, 13 September 2020, 4:13 PM What does a hydrocarbon look like? Permalink Show parent In reply to Kazi Julfiker Re: Hydrocarbon by Nusrat Jahan Fahima - Wednesday, 23 September 2020, 7:33 AM A hydrocarbon is an organic compound made of nothing more than carbons and hydrogens. ... Saturated hydrocarbons have as many hydrogen atoms as possible attached to every carbon. For carbons on the end of a molecular chain, three can be attached. For carbons in the middle of a chain or a ring, two can be attached.ID: 201-29-164323(A) Permalink Show parent In reply to Ruhul Amin (201-29-1646) Re: Hydrocarbon by MD. Nadim Hasan - Thursday, 17 September 2020, 11:55 PM Tertiary carbocations are more stable than primary or secondary carbonation because they have three methyl groups to distribute it's positive charge rather than only one or two methyl groups. ... Of course, the more the positive charge is spread out, the more stable your carbocation will be 3 degree.Id:201-29-1702 Permalink Show parent
In reply to Ruhul Amin (201-29-1646) Re: Hydrocarbon by Popy Rani Sutradhar - Tuesday, 18 August 2020, 3:22 PM because -CH3 is electron providing group. and more the number of electron providing group more stable will be carbocation. therefore 3 degree carbocation is more stable. Tertiary carbocation possess minimum positive charge due to - (1) hyper conjugation (2) electron releasing inductive effect of alkyl group primary carbanions have only one alkyl group and the increase in electron density is less on the carbon atom. Hence it is more stable thansecondary or tertiary carbanions. ... (other atom is a more electronegative atom). Permalink Show parent In reply to Popy Rani Sutradhar Re: Hydrocarbon by Mehedi Hasan Rabbi - Tuesday, 18 August 2020, 6:58 PM Why carbanion is more stable than carbonation? Mehedi Hasan Rabbi ID:201-29-1700 Permalink Show parent In reply to Mehedi Hasan Rabbi Re: Hydrocarbon by Sanjida ahmed Emma 201-29-1711 - Tuesday, 18 August 2020, 7:33 PM reactivity determined by several factors: The inductive effect. Electronegative atoms adjacent to the charge will stabilize the charge; Hybridization of the charge-bearing atom. Permalink Show parent In reply to Mehedi Hasan Rabbi Re: Hydrocarbon by kamrul hasan sujon - Wednesday, 19 August 2020, 9:14 PM carbocation is more stable. let's take for example the ter-butyl carbocation (Ch3)3-C+ this charged ion is highly stabilized due to the presence of the three donor methly groups that donate electrons, and hence largely stabilize the positive charge. On the other hand the tert-butyl carbanion (CH3)3-C- would be less stabilized and more reactive than its positive catine since The negatively charged carbon atom in carbanion is sp3 hybridized. Therefore, it has a tetrahedral structure. Three of the four sp3 hybridized orbitals form 3s-bonds with hydrogen or carbon atom of the alkyl group. The fourth sp3 hybrid orbital contains the lone pair of electrons.This would cause to bring the reactivity to this ion and makes it act as a free radicals. ID:201-29-1686 Section :23(A) Permalink Show parent
In reply to Popy Rani Sutradhar Re: Hydrocarbon by Mehedi Hasan Rabbi - Tuesday, 18 August 2020, 6:58 PM Why carbanion is more stable than carbonation? Mehedi Hasan Rabbi ID:201-29-1700 Permalink Show parent In reply to Mehedi Hasan Rabbi Re: Hydrocarbon by Sanjida ahmed Emma 201-29-1711 - Tuesday, 18 August 2020, 7:33 PM reactivity determined by several factors: The inductive effect. Electronegative atoms adjacent to the charge will stabilize the charge; Hybridization of the charge-bearing atom. Permalink Show parent In reply to Mehedi Hasan Rabbi Re: Hydrocarbon by kamrul hasan sujon - Wednesday, 19 August 2020, 9:14 PM carbocation is more stable. let's take for example the ter-butyl carbocation (Ch3)3-C+ this charged ion is highly stabilized due to the presence of the three donor methly groups that donate electrons, and hence largely stabilize the positive charge. On the other hand the tert-butyl carbanion (CH3)3-C- would be less stabilized and more reactive than its positive catine since The negatively charged carbon atom in carbanion is sp3 hybridized. Therefore, it has a tetrahedral structure. Three of the four sp3 hybridized orbitals form 3s-bonds with hydrogen or carbon atom of the alkyl group. The fourth sp3 hybrid orbital contains the lone pair of electrons.This would cause to bring the reactivity to this ion and makes it act as a free radicals. ID:201-29-1686 Section :23(A) Permalink Show parent
In reply to Mehedi Hasan Rabbi Re: Hydrocarbon by Sanjida ahmed Emma 201-29-1711 - Tuesday, 18 August 2020, 7:33 PM reactivity determined by several factors: The inductive effect. Electronegative atoms adjacent to the charge will stabilize the charge; Hybridization of the charge-bearing atom. Permalink Show parent
In reply to Mehedi Hasan Rabbi Re: Hydrocarbon by kamrul hasan sujon - Wednesday, 19 August 2020, 9:14 PM carbocation is more stable. let's take for example the ter-butyl carbocation (Ch3)3-C+ this charged ion is highly stabilized due to the presence of the three donor methly groups that donate electrons, and hence largely stabilize the positive charge. On the other hand the tert-butyl carbanion (CH3)3-C- would be less stabilized and more reactive than its positive catine since The negatively charged carbon atom in carbanion is sp3 hybridized. Therefore, it has a tetrahedral structure. Three of the four sp3 hybridized orbitals form 3s-bonds with hydrogen or carbon atom of the alkyl group. The fourth sp3 hybrid orbital contains the lone pair of electrons.This would cause to bring the reactivity to this ion and makes it act as a free radicals. ID:201-29-1686 Section :23(A) Permalink Show parent
In reply to Ruhul Amin (201-29-1646) Re: Hydrocarbon by Kazi Julfiker - Sunday, 13 September 2020, 4:13 PM What does a hydrocarbon look like? Permalink Show parent In reply to Kazi Julfiker Re: Hydrocarbon by Nusrat Jahan Fahima - Wednesday, 23 September 2020, 7:33 AM A hydrocarbon is an organic compound made of nothing more than carbons and hydrogens. ... Saturated hydrocarbons have as many hydrogen atoms as possible attached to every carbon. For carbons on the end of a molecular chain, three can be attached. For carbons in the middle of a chain or a ring, two can be attached.ID: 201-29-164323(A) Permalink Show parent
In reply to Kazi Julfiker Re: Hydrocarbon by Nusrat Jahan Fahima - Wednesday, 23 September 2020, 7:33 AM A hydrocarbon is an organic compound made of nothing more than carbons and hydrogens. ... Saturated hydrocarbons have as many hydrogen atoms as possible attached to every carbon. For carbons on the end of a molecular chain, three can be attached. For carbons in the middle of a chain or a ring, two can be attached.ID: 201-29-164323(A) Permalink Show parent
In reply to Ruhul Amin (201-29-1646) Re: Hydrocarbon by MD. Nadim Hasan - Thursday, 17 September 2020, 11:55 PM Tertiary carbocations are more stable than primary or secondary carbonation because they have three methyl groups to distribute it's positive charge rather than only one or two methyl groups. ... Of course, the more the positive charge is spread out, the more stable your carbocation will be 3 degree.Id:201-29-1702 Permalink Show parent