What is incorrect order of stability? (.I.) (.II.) (.III.) Boat form of 1,4-cyclohexandiolChairformof1,4-cyclohexandiol (.IV) (.V.) Gauche form of succine acid Antic from of succinic acid

Question

What is incorrect order of stability? (.I.) Question

(.II.)

(.III.) Boat form of 1,4-cyclohexandiol>Chairformof1,4-cyclohexandiol (.IV) Question

(.V.) Gauche form of succine acid > Antic from of succinic acid (A) I, II, V (B) I, III, IV (C) I, IV (D) I

Tardigrade Admin · Accepted Answer

In cyclic alkene up to carbon -10 , Cis is more stable than trans. In Newmann project if no H- bonding than anti form is more stable than gauchform. In CH2F-CH2F gauch is more sutable due to gauch effect.

Q. What is incorrect order of stability?

$(I)$

$(II)$

$(III)$ Boat form of $1, 4 - cyc l o h e x an d i o l > C hai r f or m o f 1, 4 - cyc l o h e x an d i o l$

$(I V)$

$(V)$ Gauche form of succine acid > Antic from of succinic acid

I, II, V

I, III, IV

I, IV

I

In cyclic alkene up to carbon $- 10$ , Cis is more stable than trans. In Newmann project if no $H -$ bonding than anti form is more stable than gauchform. In $C H_{2} F - C H_{2} F$ gauch is more sutable due to gauch effect.

Q. What is incorrect order of stability? (I) (II) (III) Boat form of 1,4−cyclohexandiol>Chairformof1,4−cyclohexandiol (IV) (V) Gauche form of succine acid > Antic from of succinic acid

I, II, V

I, III, IV

I, IV

I

In cyclic alkene up to carbon −10 , Cis is more stable than trans. In Newmann project if no H− bonding than anti form is more stable than gauchform. In CH2​F−CH2​F gauch is more sutable due to gauch effect.

Q. What is incorrect order of stability?

$(I)$

$(II)$

$(III)$ Boat form of $1, 4 - cyc l o h e x an d i o l > C hai r f or m o f 1, 4 - cyc l o h e x an d i o l$

$(I V)$

$(V)$ Gauche form of succine acid > Antic from of succinic acid

In cyclic alkene up to carbon $- 10$ , Cis is more stable than trans. In Newmann project if no $H -$ bonding than anti form is more stable than gauchform. In $C H_{2} F - C H_{2} F$ gauch is more sutable due to gauch effect.