Answer:
trans-1,3-pentadiene is more stable than 1,4-pentadiene due to presence of a conjugated double bond.
Explanation:
Here, 
H(hydrogenated pdt.) is same for both 1,4-pentadiene and 1,3-pentadiene as they both produce pentane after hydrogenation
H(diene) depends on stability of diene.
More stable a diene, lesser will be it's H(diene) value (more neagtive).
trans-1,3-pentadiene is more stable than 1,4-pentadiene due to presence of a conjugated double bond.
Hence, 
is higher (less negative) for trans-1,3-pentadiene
Answer:
Agriculture was practiced for thousands of years without the use of artificial chemicals. Artificial fertilizers were first created during the mid-19th century. These new agricultural techniques, while beneficial in the short term, had an Institute of Plant Industry to improve traditional farming methods in India.
Explanation:
Answer:
1) The risk of high cost due to increased resource requirements
2) The risk of late entry into the (a changed) market
Explanation:
The analysis being performed by the engineers = A cost benefit analysis to determine if a new technology should be developed
A cost-benefit analysis is a process of appraising or measuring the advantages, benefits of a policy, action or decision, so as to find the (equilibrium) balance point between the costs of the decision or action
The risk to be considered are;
1) The risk of high cost due to increased resource requirements
The increased cost required for the development of the new technology now which due to the unlikely existence of a similar invention in the market that will give them an advantage of increased profits
2) The risk of late entry into the (a changed) market
The changes in the consumer preferences, market landscape, and the likely introduction into the market of a similar invention by the competition in the near future which will reduce the amount of profits that can be gained from the invention
Answer:
See explanation and image attached
Explanation:
Fischer esterification is a type of reaction used to convert carboxylic acids to ester in the presence of excess alcohol and a strong acid which acts as a catalyst. Another final product formed in the reaction is water.
The mechanism for the fischer esterification of Benzoic acid and C H 3 O H in the presence of HCl as the catalyst is shown in the image attached to this answer.
The final products of the reaction are methyl benzoate, water and H^+ as shown in the image attached.
