How to determine order of bond angle of Me-O-Me, H3Si-O-SiH3 and (ph)3Si-O-Si(Ph) ?

 (1) Oxygen of Me-O-Me is sp3 hybridised so C-O-C bond angle is more than 109’28” approx 110” due to crowding of methyl group.

(2) In disilyl ether , oxygen is Sp2 hybridised and planer due to back bonding between oxygen and silicon atom.  In this back bonding lone pair of oxygen atom donate to the vacant d orbital of silicon atom  due to this fact bond lengths of Si-O is decrease and  increases (approx 140”).

(3) In (Ph)3Si-O-Si(Ph)3  compounds Si-O-Si bond angle is Approx 180 due to back bonding and hybridisation is Sp.

Related Questions:

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Nitrogen (N) atom in trimethyl amine [N(CH₃)₃] is sp3 hybridised and tetrahedral ( bond angle ~107)  due to non bonding electron pair of N is localised (more basic). On the other hand N atom of trisilyl amine [N(SiH₃)₃] is sp2 hybridised and trigonal planner (bond angle~120).This is due to the participation of non-bondlng pair of N into pπ-dπ back banding. Due to this delocalization of non-bonding electron pair of N in trisilyl amine it is also less basic

Related Questions:

Why trimethylamine amine ( N(CH3)3) is tetrahedral while trisilyl amine (N(SiH3)3) planner.?

Why trimethyl amine {(CH3)3 N:} is pyramidal while trisilyl amine {(SiH3)3N:} is trigonal planer?

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Generally neutral atom donates only one lone pair to back bonding because after that, electron density on that atom itself highly reduced but the compound [(CF₃)₂-Al-O-Al-(CF₃)₂] is a rare example of two lone pair donation.

Related Questions:

Why trimethylamine amine ( N(CH3)3) is tetrahedral while trisilyl amine (N(SiH3)3) planner.?

Why trimethyl amine {(CH3)3 N:} is pyramidal while trisilyl amine {(SiH3)3N:} is trigonal planer?

Which is/are the correct statement/s about structure of methyl isothiocyanate (H3CNCS) and Silyl isothiocyanate(SiH3NCO)?

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What are the structure of (1) N(SiH3)3 (2) {(Me)3Si}2N-Si(Me)3 (3) HN(SiH3)2 and give the Answers of following questions?

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Q (1): which is greater x or y?
Q (2): which is greater x or z?
Q (3): which have greater extent of back Bonding?

SOLUTION:

Ans: (1): ‘y’ is greater than ‘x’ because of steric repulsion of -CH₃ group.

Ans: (2): “z’ will be greater because one lone pair going two places.

Ans; (3): the extant of back bonding is 3^rd >1^st > 2nd 

Which of the following is correct order of (B-O) bond length of following compounds? (1) B(OH)3 (2) B(OMe)3 and (3) B(Me)2OH

 SOLUTION:

Extent Back Bonding is   3>1>2 and bond length order is  y>x>z  

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Why trimethylamine amine ( N(CH3)3) is tetrahedral while trisilyl amine (N(SiH3)3) planner.?

Why trimethyl amine {(CH3)3 N:} is pyramidal while trisilyl amine {(SiH3)3N:} is trigonal planer?

Which is/are the correct statement/s about structure of methyl isothiocyanate (H3CNCS) and Silyl isothiocyanate(SiH3NCO)?

What is the Si–N–C bond angle in Silyl isothiocyanate and methyl isothiocyanate (H3CNCS)?

What are the order of extent back bonding, Lewis acid character and nucleophilicity of (BF3, BCl3, BBr3, BI3)boron trihalides?

Arrange the silicon halides into decreasing order of Lewis acids Character? SiF4, SiCl4, SiBr4, SiI4

Which of the following correct statement about structure of Ortho boric acid (H3BO3 ) is/are? Statements are as