giass ture (Tg) is the temperature range where a polymer chain gains of the polymer chains depends on (1) the presence of stiffening ated in the polymer backbone and (2) the presence of functional backbone. These functional groups attached to the polymer back For example, polyethylene terephthalate (PET) has a higher glass tra ene adipate. The terephthalic acid moiety in polyethylene ably an inflexible unit. Furthermore, the terephthalic acid moie e and restricts polymer chain mobility. On the other hand, the ene adipate is flexible; thus, making the polymer backbone chains pendant groups in the glass transition temperature is very evident n temperatures of low density polyethylene (LDPE) and polyvinyl al higher glass transition temperature than LDPE attributed to the p OH) which can form strong hydrogen bonds with other polymer ch

Can you help me part B? Which is the formula of this rule of reaction? I don't know which was the rule of the reaction?

Draw the structure of the major organic product(s) of the reaction. HCI HO. • You do not have to consider stereochemistry. • All carboxyl and amino groups should be drawn in the neutral form. • If no reaction occurs, draw the organic starting material. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the + sign from the drop-down menu. ору aste С ChemDoodle Previous >

Draw the structure(s) of the major organic product(s) of the following reaction. H H You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • Do not include lone pairs in your answer. They will not be considered in the grading. • If no reaction occurs, draw the organic starting material. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate multiple products using the + sign from the drop-down menu. 1. LIAIH4 / dry Et₂0 2. aqueous HCI 2 OOD OO. [F ChemDoodleⓇ < 26

Can you help me with part A and part B, please?

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e) emulsifiers are pretty important compounds for daily life, externally and internally to us humans. Describes the two parts of an emulsifier molecule, and how most emulsifiers work and what they actually do.

for the reactants: ester and enolate ion. • Assume all esters to be ethyl esters. . Do not include counter-ions, e.g., Nat, It, in your answer. • Draw the enolate ion in its carbanion form. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate multiple reactants using the + sign from the drop-down menu. ? O-Sn [F

Consider propanoic (CH3CH2CH2CO2H) acid and pentanoic (CH3CH2CH2CH2CO2H) acid and the corresponding alcohols with the same number of carbons, propanol (CH3CH2CH2COH) and pentanol (CH3CH2CH2CH2COH). Select the class of compound that is more soluble. {one answer] Select the best explanation for your answer to the previous question. [a second answer] Group of answer choices a. The solubility of alcohols in water decreases with increasing chain length. b. Propanoic acid and pentanoic acid are more soluble in water than the corresponding alcohol. c. Carboxylic acids are generally more soluble in water than alcohols of the same chain length because of increased hydrogen bonding with the -COOH functional group.  d. Propanol and pentanol are more soluble in water than the corresponding carboxylic acid e. The solubility of carboxylic acids in water decreases with increasing chain length. f. Alcohols are generally more soluble in water than carboxylic acids of the same…

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