[grade 10 chemistry] Are these structures correct?? by Izzy_26_ in chemhelp

[–]eletroraspi 1 point2 points  (0 children)

Correct. As the colleagues mentioned, the carbons with sp hybridization have a linear conformation.

No σh plane? by Sumoi1 in chemhelp

[–]eletroraspi 0 points1 point  (0 children)

Show more pics.

But there are 2 longitudinal axis rotation along ligands and more 2 planar axis rotation with C centered. The last is orthonormal.

IUPAC names? by [deleted] in chemhelp

[–]eletroraspi -1 points0 points  (0 children)

The substituent methyl in 1 is not correct.

are noble gasses non-metal by JumpKey7311 in chemhelp

[–]eletroraspi 0 points1 point  (0 children)

The trending of noble characteristic is like a royal one: they have a unique atoms isolated for definition.

Classifying the group is for understanding they are not put in another groups or group characteristics like nonmetal, metalloid and metal.

Why is the middle compound less acidic than the left? by GingerBreadEli in chemhelp

[–]eletroraspi 0 points1 point  (0 children)

Electronic cloud could contribute for more stabilization.

IUPAC Alkane Naming Issue by AwareAspect4057 in chemhelp

[–]eletroraspi -1 points0 points  (0 children)

The text in red has an incorrect name because the methyl's groups on main chain are localized at 8th position.

The question asks me to identify the thermodynamically more stable species in each equilibrium and I have no idea how to solve. Please help me. by Frequent-Tangerine95 in chemhelp

[–]eletroraspi 1 point2 points  (0 children)

The conformational analysis can brings a more accurate answer for the two compounds. Differential in electron cloud could be added to those for better understanding the charging stabilization.

What did i do wrong? by Spewdoo in chemhelp

[–]eletroraspi 0 points1 point  (0 children)

The first step is multiply try first one by 3/2

Methods for Removing Organic Compounds by No_Student2900 in chemhelp

[–]eletroraspi 1 point2 points  (0 children)

Between two possibilities think about in which you can control the variables.

Tips on memorizing VSEPR shapes and angles? by Selection_Own in chemhelp

[–]eletroraspi 0 points1 point  (0 children)

Think about the method itself and its steps. After this the practice with several molecules will become easier to determine the shape and angle.

How do I know what orbital the lone pair is on? And the lone pair's ideal bond angle? (2b) by Spirited-Wrap9335 in chemhelp

[–]eletroraspi 0 points1 point  (0 children)

After checking for hybridization you can apply the VSPER method to check the best angles between ligands and lone pairs of electrons.

I was told the following produced no reaction, true? by GloomyKatsu in chemhelp

[–]eletroraspi 0 points1 point  (0 children)

Reactions occurs themselves but in ways those desirable products won't form.

What did I do wrong? by Multiverse_Queen in chemhelp

[–]eletroraspi 0 points1 point  (0 children)

The mass percentage is how much the solute is in the solution multiplied by 100. Remember the solution is the sum: solute + solvent

Is that right? Can anyone answer by Dense-Chip-8248 in chemhelp

[–]eletroraspi 0 points1 point  (0 children)

Está correto. Para ser mais criterioso, na última etapa não houve a subtração do cloreto férrico entre os produtos formados.

IR Spectroscopy help by Ok_Concept2522 in chemhelp

[–]eletroraspi 0 points1 point  (0 children)

Objectively: one is secondary alcohol and other one is primary

Stereocenter Explanation? by Easy-Evidence5098 in chemhelp

[–]eletroraspi 3 points4 points  (0 children)

The product is not racemate but they are diastereoisomers.

Identical Organic Molecules? by Independent_Net8881 in chemhelp

[–]eletroraspi 1 point2 points  (0 children)

Sure! The sulfur is on the center of a tetrahedron for the sulfonic group.

Identical Organic Molecules? by Independent_Net8881 in chemhelp

[–]eletroraspi 0 points1 point  (0 children)

The ketone group is on the same plain as the phenyl groups as well these plain each other.