We are currently struggling to cover the operational costs of Xtremepapers, as a result we might have to shut this website down. Please donate if we have helped you and help make a difference in other students' lives!
Click here to Donate Now (View Announcement)
Each F only needs one more electron, they can't accept a lone pair from the Cl atom.
One simple guideline is to explore the possibility of a covalent bond first before considering using dative bonds.
ClF4(minus1).gifwhat will be the structure of ClF4-?
How to name organic compounds with more than one functional group?
which functional groups are chosen as to give them the least number? and is it necessary for both or all of the functional groups to be on the longest chain ?
http://maxpapers.com/wp-content/uploads/2012/11/9701_s09_qp_2.pdf
variant 1
qs 2)ii) Why do we add to find the enthalapy change? why nt subtract?
suppose if there is a compound with carboxylic acid and ketone group.. so I'll try to name as such both the functional groups are a part of the longest chain..? and if thats not possible, at least carboxylic acid should be .. right?When there are more than 1 functional groups, there is a need to rank the functional groups.
http://www.masterorganicchemistry.co...-nomenclature/
suppose if there is a compound with carboxylic acid and ketone group.. so I'll try to name as such both the functional groups are a part of the longest chain..? and if thats not possible, at least carboxylic acid should be .. right?
Moreover what's the use of the prefix??? for example ester prefix is ''oxycarbonyl'' and aldehyde's is OXO but we do not use these terms to name esters/aldehydes right? so what is their purpose
http://www.chemguide.co.uk/mechanisms/nucadd/hcntt.htmlIn the reaction of HCN with Carbonyl compounds, we use NaCN as a catalyst or as a source of CN- ions?
In the reaction of HCN with Carbonyl compounds, we use NaCN as a catalyst or as a source of CN- ions?
While making displayed formula, do we have to take care of making the right structure with the correct bond angles too? for example in J10/23Q5 part a, the structure given in the Marking scheme is absolutely perfect in terms of the bond angles etc but when I make displayed formulas generally I tend to just display all the bonds ( not caring about the bond angles)
So is my method acceptable?
It seems correct to me, as for balancing of the stuff in the box it's better to do it but it won't affect your answer.is my cycle correct? (particularly the highlighted part) and do we need to balance it?
For almost 10 years, the site XtremePapers has been trying very hard to serve its users.
However, we are now struggling to cover its operational costs due to unforeseen circumstances. If we helped you in any way, kindly contribute and be the part of this effort. No act of kindness, no matter how small, is ever wasted.
Click here to Donate Now